| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03930 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:236325880-236328000 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIC | MA0687.1 | chr1:236326962-236326976 | TTCTTCCTCATTTT | - | 6.42 | | ZNF263 | MA0528.1 | chr1:236327236-236327257 | CTCCCATCTCCTCCCACCTCC | - | 6.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_59322 | chr1:236304325-236328173 | Ly3 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I236162 | chr1 | 236326267 | 236327471 |
|
Enhancer Sequence | ATGCTGTGTG CAGCCTAGGG ACTTCGTGCC CTGTGTCCCA GCTGCTCCAG CCATGGCTGA 60
AAGGGGCCAA CGTAGAGCTC GGGCTGTGGC TTCAGAGGGT GGAAGCCCCA AGCCTTGGCA 120
GCTTCCATGT GTTATTGAGC CTGCAGGTGC ACAGAAGTCA AGGTCTGAGG TTTGGGAACC 180
TCCGCCTAGA TTCCAGAAGA TGTATGGAAA TGCCTGGATG CCCAGGCAAA AGTTTGCTGT 240
GGGGGTGGGG CCCTCATGGA GAAGCTCTGC TAGGGCAGTG CAGAAGGGAA ATGTGGGGTC 300
GGAGCCCCCA CACAGAGTCC CTACTGGGGC ACTGTCTAGC GGAGCTGTGA GAAGAGGGCC 360
ACTGTCCTCC AGACCTCAGA ATGGTATATC CACCGACAGC TTGCACTGCG CTCCTGGAAA 420
AGCCACAGAC ACTCAACACC AGCCCGTGAA AGCAGCCGGG AGAGAGGCTG TACCCTGCAA 480
AGCCACAGGG GTGGAGCTGC CCAAGACCAT GGGAACCCAC CTCTTGCATC ACTGTGACCT 540
GGATGTGAGA CTTGGAGTCA AAGGAGATCA TATTGGAGCT TTAAACTTTG ACTGACCTGC 600
TGGATTTCAG ACTTGCATGG GCCCTGTAAC CACTTTGTTT TGGCCACTTT CTCCCACTTG 660
GAACGGCTGT ATTTACCCAA TGCCTGTATC TCCATTGTAT CTAGGAAGTA ACTAGCTTGC 720
TTTCGATTTT ACAGGCTCAT AGGCAGAAGG GACTTGCCTT ATCACAGATG AAACTTTGGA 780
CTGTGGACTT TTGGGTTAAT GCTGAAATGA GTTAAGACTT TTGGGGACTG TTGGGAAGGC 840
ATGATTGGTT TTGAAATGTG AGGACGTGAG ATTAGGAGGG GCCAGGGATG GAATGATATG 900
GTTTGGCTGT GTCCCCCTCC AAATCTCAAC TTGAATTGTA TCTCCCGGAA TTCCCATGTG 960
TTGTGGGAGG GACCTGGGAG GAAGTAATTG AATCACGGGG GCCGGTCTTT CTTGTACTAT 1020
TCTTGTGATA GTGAATAAGT CTCAGGAGAT CTGATGGGTT TATCAGGGGT TTCCGCTTTT 1080
GCTTCTTCCT CATTTTTTTC TCTTGCTGCT GCCATGTAAG AAGTGCCTTT CGCCACCCAC 1140
TGTGATTCTG AGGCTTCCCC AGCCATGTGG AACTGTAAGT CCAATTAAAC TTCTTTTTCT 1200
TCCCAGTCTC AGATATGTCT TCATCAGCAG CATGAAAACA GACTAATATA CCTCCTCATA 1260
CCTCCCATGC CTCCACACTT TTCACACTTC CTCACACCTC CCATACTGCC TCACACTTCC 1320
CACACCTCCC ATACCTCGAC ACACTTTTCA CATCTCCTCC CATCTCCTCC CACCTCCCAC 1380
ACCTCCCCAT GCTTTCAACA CCTCTCATAC CTCCTCACAC CTCCCATGCC TCCTCACACT 1440
TTTCAGCACC TCCTCACAGC CCCCATGCCT CTCCACACCT CCCCATGCCT CCCCACACCT 1500
CTCACACTTC CTACACCTCC TCACACCACT GGTGCTTATT ACTGACATGT CTGTCTGCCT 1560
GTGTATTTCT CTGGGACAGG CCCAGCTTCT CCTCCTTTTT ACAATTCTTG GGTCCAACCC 1620
AGGGTCTGAT GCAGACTCAG TGCTGAGTAT CAGTTGACCT GACTTGAACA CCACCAATTG 1680
GAAAGCCAGG ATGATGTAAA TTTTCATCTG GCCTCATTTG TTCCTTAGCC TCTCATAGGG 1740
GTCACACCTC CCTCTTTTTC ATTCTTGTAC ATCTGGGGAC ACTGAGCAGG AGGTGCCCGT 1800
GCTGTCAAAG CACCAGAGAG TATGACAGCA GAATTCACGT CTGCCTCCCC ACAGGAGCCG 1860
TCGCCCCTCC CAGCTGAGTT CCTGCCAAGG TCAGTGGGAG CCAGTGCAGA CTGGCAGAAA 1920
TGGGCAGCCG GATATGAGAG CCCAGCCGGC CAGAGAGCCA GGGTGAGCCA GGAGCTTTAG 1980
CTCAAGTTCC GGACACCCAC CAGTCTTTAG CAAAGTCTCT CAGAACACAG AGGGGAGTGG 2040
GTGGGAGAGT TTAGATTTTT GTTTTTGAAA ACTTGGTTTA TGCCCTTTAA TTAATGAGGG 2100
CAAAAGTTGT ACTGAAATTA 2120
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