| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08832 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr13:106642780-106644640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr13:106644268-106644278 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr13:106644268-106644278 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr13:106644268-106644278 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr13:106644268-106644278 | AACAGCTGTT | - | 6.02 | | Myog | MA0500.1 | chr13:106643662-106643673 | CTGCAGCTGTT | - | 6.02 | | NEUROD2 | MA0668.1 | chr13:106643391-106643401 | ACCATATGGC | - | 6.02 | | NFIC | MA0161.2 | chr13:106644247-106644258 | TCTGCCAAGAA | - | 6.02 | | RORA(var.2) | MA0072.1 | chr13:106642969-106642983 | TTGACCTAAATTAA | - | 6.01 | | Tcf12 | MA0521.1 | chr13:106643662-106643673 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34149 | chr13:106642640-106645099 | HCC1954 | | SE_36583 | chr13:106641912-106645243 | HMEC |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I105989 | chr13 | 106642150 | 106644938 |
|
Enhancer Sequence | TGGTTGGGGT TGCCCTGTGC CTCACAGGAT GTTTTCCCAC TAGATATCAG TAGCACTCCC 60
TGGCTCCAGA TGGGACAACC AAAGTGTTTG CAGACATTCC CAAATGTCCC TTGTGGGGTG 120
GGGTAGGGGA GTGGTAAAAT TGCCCTGCTT GAGAACTACT GAATTCTAAC TGCATGTCCT 180
GCCAGCCATT TGACCTAAAT TAAATTCTTC CCCCAAATAT CCCATTTTTC TCACTTCCTT 240
ATTTCTCTTT GTGGGTCTAA TTTTTCCTCA GTCGTTCAAG CTCAACATGT CTGTGCTATG 300
TCTGACTCAG CCCCCACCCC CCATCCTCCA CACCCAACCC ATCACTAAGA CTCATAGCAT 360
TGACTTCTAC TCCCAAGCCC CTCCTTCCCT TTCCTGTTTA TCTTTTAGAT TCTGGCCTCT 420
GTGATCTCAC ATTAACGCCA ATAGCTTTTT TCTGGTTTCC CTATCATTAA TTCATCCTAT 480
CCAGTGATGA TAGATAAGGT TTTCTCAAAG GTAGCTTGTA GTATGTTCCT TCTTTCATTA 540
GAACCTTCAG TGTTTCCCAA TGATAGACCA AATTAAGTAC AAATTGCTCA CTCTTGCATT 600
TCAGAGCCTC CACCATATGG CACCAACTCC CTTTCCAGTC TCAGTTCACA CATCTCCTCT 660
ACAAGTACCA ACAGGGTGGC TCACTGCTCA TCAAAAGTGG GCTATGCATA TGCCCTGATG 720
CCTTTTTCTC ATGCTGTTAC CTCACTTGGT GAGTTCTCCT CCACAATGTT CCCCTAAAAA 780
AGCTCACTCT TCTTTCAAAG CCAGTCTGAT ATTCCACAAT ATTCACAAAT CATTTTTTTC 840
TGGTTGACCC AACAGAATGT ATTCACTTTC CCATCTGAAT CTCTGCAGCT GTTCATACTG 900
CCTCTTCTGT CAGGTTACAC ATCATCCCCT GGTATAGCCC GTGTAGTGTT AATAGTATCT 960
GCTTTGCCAG ATTGTAATCT TAATGATGGC AGAACTATGG TCATATTCTT CTTCATACAC 1020
TCTAGTATTT AGCACAGCTA TATGCATTTT AGATGTTCTT AATTATTTGT CTAAATGAGT 1080
AATAACAGTG AACTTACCTG CTTACTATCT TAACACAGTT CCTCACCATT CTTTTCTTAA 1140
ATAATTGGTT TCTCAGCTGG TCTTTTGACT CATGTCTTTC CAACCCATTC TCTGCCTGGT 1200
ACAAAAGTCA CTTTCCAAAC ACAAGTCTGA TCATGCTGAC CCTGACTGAG AACTTGGAAT 1260
GGCTCCCGTT GCCTAGAGGA TGGGTGCAAA CTCCTTGGTA TGACACACAA AGCCCTCTGT 1320
ATTCTGGCTA CTGTGGTTTG TCTCAGCAGT CCTCCCTCCA ACTGCATTCT TGCGACATGC 1380
TAAGTTTCCA GTTCCAGCTG TCACGCTGCT CCTTTCCCCA CATCTCCCAT ACCTTTGTTT 1440
GTACTGCTCC TTCTGCCAGG AATGCCTTCT GCCAAGAATG CCACCTACAA CAGCTGTTTA 1500
CTTCTCACTA CTATGCAAGG AGGGCCCTGG CCTTCCACAC CATGAGCCTC CTTCCAGGGG 1560
CATCCACTGG GCTCTGCACG TACTCCTGCC ACAGCTCCTG TAATATTTTG CTGTGTTGAC 1620
TTTTCATGCC TGAATCCAGC TGCTCACAAT GAGCACATAG AGCAAAATGA ACTGTGTTTT 1680
ATAGTCCTTT GCCTTTCAGA TGCCTAGATA GTGCTGACAA TGGAGGAAGC TAATGAAAAC 1740
TATCTTGCCC AATGACTGAT GAATGGATGA ATCCAAAGCA GAAAACCAGT CTATTCTAGT 1800
CACCAACTAG AAGAGTTTGT TTCATAGATT ATGTATGTCA GTGTTTAAAA TGCCACCAAC 1860
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