| Tag | Content |
|---|
EnhancerAtlas ID | HS133-11820 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:75337750-75338920 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr16:75338209-75338223 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_02649 | chr16:75338051-75341124 | Astrocytes | | SE_28243 | chr16:75337321-75345603 | Fetal_Intestine | | SE_29161 | chr16:75337343-75345706 | Fetal_Intestine_Large | | SE_34217 | chr16:75338011-75341238 | HCC1954 | | SE_36578 | chr16:75337563-75341440 | HMEC | | SE_44521 | chr16:75337481-75341198 | NHDF-Ad | | SE_46210 | chr16:75337419-75341171 | Osteoblasts | | SE_53350 | chr16:75337445-75341237 | Spleen | | SE_64737 | chr16:75337963-75341441 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I075303 | chr16 | 75337402 | 75345344 |
|
Enhancer Sequence | CAGTATGCTG GTGGAGAAGA GCTTACTGGT AAGAAGCAGA GCTGCCGAGC AGCCAGGGCT 60
CTCTGGTGGG ACACTCAACA TTTCCTTTCA TGGCTAGGGG TGAGGACTGT TGATTTTGAG 120
CCATGAAGCC ACTTCTGTGG TAACTTCCTT AGTGCCTTCT GAGGTCCGTA AGTACTTATG 180
AACACCTTTT CTTTCTTTTC TTTTCCTTTC TCTCTCTCTC TCTCTTTCTT TCTTGATACA 240
CAGTCTTGCT CTGTCACCCA GGCTGGAGTG CAGTGGTTCA GTCTTGGCTC ACTGCAACCT 300
CCACCTAGTG GGTTCAAGTG ATCCTCCTGC CCCAGCCTCC CAAGTAGCTG GGATTACAAG 360
TGTGCACCAC TATGCCTGGC TAATTCTTAT ATTTTTAGTA GGATGGGGTT TTGCCAGGTT 420
GGCTAGGCTG GTCTCGAAAT CCTGACCTCA AGTGATCTGC CCGCCTCGGC CTCCGAAAGT 480
GCCAAGATTA CAGGTGTGAA CCACCATGCC TGGCCACCAT TTCTTTCTTG ATTTTTTGTT 540
TAATCACCAG TAAGACAAAT ATGACAAGGA AAGGACCCTT TTTACAACTG AATACGTAGG 600
TTATGAACAT TCTCTTTGTA TTCCACAGCG AAGAGAAAGA GGTGCAAGTG ATGGCCTGGG 660
GTGCTGTCTG AGGGCCTGGC CTATCACACA GGCTATAGCC AAGGGTAAAG CCCCACCCCA 720
GGCCATAATG ACACAGACAA AAAAAAATTC ACAATAATGC AACATCTAGG CATTCCATTG 780
GCTCAGTTTT TGACGGATCT GAACTAGTTT GGTTTCTCAG AAGGACAAAT GATTCAGATA 840
AGGCCAAGGC TGCTACCACA GGCCAGATCC AACCACTAGG CAACTTACAG TTCACTGGAG 900
CTGTAATTCA GCAAATTCAG CTTGGCAGAT GTGACTGGCC CCTGAGAGTA CTCCTCACAT 960
GCCCCGCCTT CCCTCCACCC GCAGTGGCCT TCCCAGTGAC AGGCCCTGCC CCACACTGGA 1020
ACAGAGACTT ACTGACAAAC CAAAGTGCTC ACATTTTTAG TTCCATCATG AAAAGCTCCT 1080
GCTTGCTTAC AGTGGGCAGT TTGTCTCCAA TAAATCATTT GATTTCAGGG TTCTGAGGAT 1140
TTTCCAAGGC ATAAAACCTA CTCCTTCTTA 1170
|
