| Tag | Content |
|---|
EnhancerAtlas ID | HS002-02927 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr13:106642740-106644530 |
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 | ACCTTAACCC TATTGACATT TTGGGTCAGA TGAGTCTTTG TGGTTGGGGT TGCCCTGTGC 60
CTCACAGGAT GTTTTCCCAC TAGATATCAG TAGCACTCCC TGGCTCCAGA TGGGACAACC 120
AAAGTGTTTG CAGACATTCC CAAATGTCCC TTGTGGGGTG GGGTAGGGGA GTGGTAAAAT 180
TGCCCTGCTT GAGAACTACT GAATTCTAAC TGCATGTCCT GCCAGCCATT TGACCTAAAT 240
TAAATTCTTC CCCCAAATAT CCCATTTTTC TCACTTCCTT ATTTCTCTTT GTGGGTCTAA 300
TTTTTCCTCA GTCGTTCAAG CTCAACATGT CTGTGCTATG TCTGACTCAG CCCCCACCCC 360
CCATCCTCCA CACCCAACCC ATCACTAAGA CTCATAGCAT TGACTTCTAC TCCCAAGCCC 420
CTCCTTCCCT TTCCTGTTTA TCTTTTAGAT TCTGGCCTCT GTGATCTCAC ATTAACGCCA 480
ATAGCTTTTT TCTGGTTTCC CTATCATTAA TTCATCCTAT CCAGTGATGA TAGATAAGGT 540
TTTCTCAAAG GTAGCTTGTA GTATGTTCCT TCTTTCATTA GAACCTTCAG TGTTTCCCAA 600
TGATAGACCA AATTAAGTAC AAATTGCTCA CTCTTGCATT TCAGAGCCTC CACCATATGG 660
CACCAACTCC CTTTCCAGTC TCAGTTCACA CATCTCCTCT ACAAGTACCA ACAGGGTGGC 720
TCACTGCTCA TCAAAAGTGG GCTATGCATA TGCCCTGATG CCTTTTTCTC ATGCTGTTAC 780
CTCACTTGGT GAGTTCTCCT CCACAATGTT CCCCTAAAAA AGCTCACTCT TCTTTCAAAG 840
CCAGTCTGAT ATTCCACAAT ATTCACAAAT CATTTTTTTC TGGTTGACCC AACAGAATGT 900
ATTCACTTTC CCATCTGAAT CTCTGCAGCT GTTCATACTG CCTCTTCTGT CAGGTTACAC 960
ATCATCCCCT GGTATAGCCC GTGTAGTGTT AATAGTATCT GCTTTGCCAG ATTGTAATCT 1020
TAATGATGGC AGAACTATGG TCATATTCTT CTTCATACAC TCTAGTATTT AGCACAGCTA 1080
TATGCATTTT AGATGTTCTT AATTATTTGT CTAAATGAGT AATAACAGTG AACTTACCTG 1140
CTTACTATCT TAACACAGTT CCTCACCATT CTTTTCTTAA ATAATTGGTT TCTCAGCTGG 1200
TCTTTTGACT CATGTCTTTC CAACCCATTC TCTGCCTGGT ACAAAAGTCA CTTTCCAAAC 1260
ACAAGTCTGA TCATGCTGAC CCTGACTGAG AACTTGGAAT GGCTCCCGTT GCCTAGAGGA 1320
TGGGTGCAAA CTCCTTGGTA TGACACACAA AGCCCTCTGT ATTCTGGCTA CTGTGGTTTG 1380
TCTCAGCAGT CCTCCCTCCA ACTGCATTCT TGCGACATGC TAAGTTTCCA GTTCCAGCTG 1440
TCACGCTGCT CCTTTCCCCA CATCTCCCAT ACCTTTGTTT GTACTGCTCC TTCTGCCAGG 1500
AATGCCTTCT GCCAAGAATG CCACCTACAA CAGCTGTTTA CTTCTCACTA CTATGCAAGG 1560
AGGGCCCTGG CCTTCCACAC CATGAGCCTC CTTCCAGGGG CATCCACTGG GCTCTGCACG 1620
TACTCCTGCC ACAGCTCCTG TAATATTTTG CTGTGTTGAC TTTTCATGCC TGAATCCAGC 1680
TGCTCACAAT GAGCACATAG AGCAAAATGA ACTGTGTTTT ATAGTCCTTT GCCTTTCAGA 1740
TGCCTAGATA GTGCTGACAA TGGAGGAAGC TAATGAAAAC TATCTTGCCC 1790
|
