| Tag | Content |
|---|
EnhancerAtlas ID | HS133-27035 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:43846020-43847500 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr6:43846217-43846229 | TGCCTGGGGGCA | + | 6.04 | | KLF4 | MA0039.3 | chr6:43846046-43846057 | CCACACCCTCC | + | 6.32 | | ZNF263 | MA0528.1 | chr6:43846353-43846374 | TGAGGAGAAGGAGAGAGAGAA | + | 6.43 | | ZNF263 | MA0528.1 | chr6:43846959-43846980 | GGAGGATGGGGCAAGGGAGGG | + | 6.5 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65246 | chr6:43845858-43847652 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I043878 | chr6 | 43845859 | 43847652 |
|
Enhancer Sequence | GCTGCTCCCT CTAGTGACAA TGCCCCCCAC ACCCTCCCCT TCTCATTTGG TAACCCCCAT 60
ACATTTTTCA AAACTCATCT CAACAGCCCC TCCTCCAGGG AGCCTTCTTC CCTCCCCAGG 120
CAGGACGGGG ACTCCGGACT CCCGGCACAC ACCTCCACTG GGACTATTCG GCCTGCGGTG 180
ACTGCATGCC ACTCGCCTGC CTGGGGGCAG AGGCTGTGTC TTATTGCTTC TGTGCTCCCA 240
GGACCCAGCA CAGTGTACAG TACAGAAAAT ATGTGTTGAC TGAATAGAAG GGAGAAGAGG 300
CAAAAGAAAT AGGGAATAAG AGGGAGAAAA GAGTGAGGAG AAGGAGAGAG AGAAGTGCAG 360
GCTGGGGCCA GTGGGGTGCA GGGGCTCAGT GAGGGCCATA CTATGAGGCG TGCGAGGGGC 420
TGCTTCAGGC TGGAACTGGG AGCACAGATT CCTCCAGTCC TGGAGGCCCT GGCCCCAGTT 480
ACTCTCCTTG GGGCCAGTGT CCTAAGTGGG GAGAGGCCAT CTGGCCTGTT ATTCAGTGGC 540
ATCTGTAGAT GGTCTGTTTT GTGCCTGGCA CTGTGCTGGG CACAGGGCTG CTGGTCTCCA 600
CCAGCTGCTC TGGCAGCCGG GATCAGAGTG ATGGGGAGCA AGATCCTTCC AGGCATCTGC 660
AGCTCTGAGG AAATGATCTG CCCATCTCTG AACAGCAGGC CTCACCCAGG ATCTCTGCCC 720
ATGGCCTTGG CTGGCACACT TCCCAGGGGA CGTTGCATGG CAGGAACACC ACTGGAAGCT 780
GCGAAGCCCC GTCAGTCCTG CCCTGCTTGC TTCTCATCCC TGTAGGAAGC TCTGAGAGGA 840
GGTGTGGAGG CTTCTCTTGG CTCCTTTTGG GATGTAGCTC CTGGCTCCCA CCCAGGCTGG 900
CTCCTCACTT GCCACCCCTA CACACACCCC AGCCCCAGGG GAGGATGGGG CAAGGGAGGG 960
GAGGGAGTCA GCCAGCCGGC TGCTGCCTGG CCTGGTAATG AATCGTCCCA AAGTTTGCTG 1020
CTCTGGCTGA ATAGCTTCCC TTCTGAAAGG GGCTTGTGAC AAAGGGGACA TTGACATCCT 1080
CCACTAGACA AGGAGGGCCG CAGGCATGCA CAGGGGAAGG CCCTTTGGGA GACGGCGGGA 1140
GGCAGCTGCG GGGATCCTGA CGTGCTGCCA CTGACTCTGC CTGATGGGCT TGGCTGGGTC 1200
TGCCTCCTTC CTGATTCTGG CACTGAAAGG CCTCAGGACT AGGGTGTCTG AAGTGACAGA 1260
AGATCTCCTT GGGAGCCTCT GTGACCCACA GTGACCAGCT GAGTTGGGGC AGGGACCAGG 1320
GAGAGGTGGA AGGGGGTCGG GAGTGGAGCA GAGCTGGCTC ACGCAGAGCA CTGGGCTGTT 1380
CAGCTGAGAA CTTAAAATGT AGCCTACCTT CGCCGGACAC TTCTTCTCCT GGGGTCCTGA 1440
TGGCCAGGAT GCTCCCCTGG CCTCCTCCAG ACCCTGGCAC 1480
|
