| Tag | Content |
|---|
EnhancerAtlas ID | HS133-07395 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:46653640-46655090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr12:46654814-46654824 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr12:46654814-46654824 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr12:46654814-46654824 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_10925 | chr12:46650125-46666583 | CD20 | | SE_18534 | chr12:46653319-46666700 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19333 | chr12:46653481-46654070 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_22331 | chr12:46653145-46666730 | CD8_primiary | | SE_34883 | chr12:46653344-46656103 | HeLa | | SE_36548 | chr12:46653450-46656417 | HMEC | | SE_64686 | chr12:46653794-46656695 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I046260 | chr12 | 46653305 | 46656077 |
|
Enhancer Sequence | GAACTATCAT CACACCCCTC TCTTTACTGC TAGCAGTCTC TAAACTACTT GCTCCTGCCA 60
CCACTCCCCT GAAATCATGC CTGATTAGGA AATTCTGGCT CCACCACTTA GAAGCTGTGT 120
AGCCCCAGGA AAGAAGGTTA ACTTCTCTTT GCCTTAGTTT CCTCATCTGT AAAATGGACT 180
TAAAGCAATA CCCATCTGAT ACAGTCATAA AGATTCCATG ACTTGGTCCA TGTGCAGCAC 240
TTAGAACAGC GTCTGGCCCG GGTTTTGTAA ATTATTGTGA CCATTGTTCC TGTTTTCTGA 300
CTTCTCCCAA ATAACTCCAC ACTGCATCCT CCCAAGACCT TCTTGGTCTC CTCTGCCAGA 360
TCCCTCCTCC TCCCAACTTT CTGTGTAGAA GTAGCTCTTT GGGCCTCGAC TCTTCTTGCT 420
CCACATATTC CAAATTCTTT CCTTTTTAGG GCTTCAGGGC TGTAGTGTCA AGTTTCATTC 480
TACAAAGGCA TCTTTCAGAT CTTTCTTCCC AGTCTTTTTC ACTTTATAAA ACTAGAATTC 540
CTTTGCGTTA TGAAATAGGA TCTCCCTCAT AAATACAACT TGATCATGAT CATGCCACTT 600
AACATGTCAC ATGTTTCTTC ATCTGTAAAA TGAGAGGGCA TGAAAGAGAG GTTATCTCTC 660
AGGTTCTTTC CTTCTCAGAA ACATTTCCAT AAATTCTTTT CAGACTCCTG CTGCCTTCTG 720
GACTGCTCCA TTAGGATGTT TATCATTACC TCAGATTCCA CATGCCTGAA GCAGAACGCA 780
TCACCTGACC TCACATGCCA GCATTCTATT TCTGTTAAAG ATATAATGCA CCTTCTCCTT 840
GTCACTCAGA CTTGAAACTT GAGTATGGCT TTCATACAAC CTCATATCTA ATCAGTTGCC 900
AAGTCCTGCC AACATTCCTT CACAAAATCC TTTTCCTTTC CCTTATTCCT TACAGTTTCA 960
CAGCCTGAAC TTTGCCACAG TCACTCTCCG CCACGCTACC TCCTGCTTCT TGCCCTCTCC 1020
CACCTATAGA GGCAGATTCT TCCTGAAAAG ACAGTCTTGC ACATTCCTCT TTCTGCCTTG 1080
CCAATCATAA CTGTTCCCTC TACAGGATGA GGTCTAATCT CTAGAACCTC AGACAGCTTT 1140
CTCTTTAATT TATGCTCCCA CTATATTCCT TCTAATTTTC CATTCCTGCA ATGGGTCTAC 1200
TCTTATGCAG TTTTCTGCTT TGTTCACACC ATCCCCCTGA TCCTGGACAC ACCCTCTCCA 1260
CCTTCCCATG AAGCCTATGC TAACTTAAGT ATGACCTTTC TTTCAAAGCC CAGCTTGCTT 1320
GCTTTTTTAA AAAATTCAAG CCAACTCTTC TGTGATGCCT TTCTCCAATG ACCAACGCAG 1380
GCATTGCCAA ATACCTCCTG GGGGCAGGGA GAGGGACATA ATTGTTCCAG TTGAGAACCT 1440
GCTTGACTGT 1450
|
