| Tag | Content |
|---|
EnhancerAtlas ID | HS133-28384 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:44748670-44750760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LHX2 | MA0700.1 | chr7:44748994-44749004 | GTTAATTAGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_40682 | chr7:44749570-44752354 | Left_Ventricle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I044710 | chr7 | 44749907 | 44750930 |
|
Enhancer Sequence | GTCTGCTGTG TCTTTCTGTC TGTTCTGCCT TCTCCCCTGA GGGGATGGGG ATGGGCCAGT 60
CCCCTCCTAA CCCACCTGGG AAGCAGCCCC CTCCTCATTG GACAGGGGGA GTGATGACCA 120
CCACCTGCAG GCCCTCGCCG GCAAAGCCGT CATTGTGAAT GCGGCAGAGG CGGCCTGGGC 180
TGCCGGGCTG TTTGGGTGCA GTCCTGTTTC TGAGCTTTCC CTGCTCTGGG TCCTTCCCCT 240
GGCTCCACCT TGAAAAAGTA CTCTGCACTC TGTGCCTCTC CGTTTGAGCC AGCGTGCCTG 300
CGGGTTCACC CTAACCACAC GTTTGTTAAT TAGTGCTCCC CAGAGCCCAA GCAACGATTC 360
CAACCTGGAG ATGGGGCCTC TCACCAGCAC ACACCTGGGT CCCCTCTGGC CAAGAGCTTC 420
ATCCCATAAC AAGCCAGGTA TTGGCTTCCT GAGCACTCAA CCAATCTCAC CCCTGAGGAA 480
GAGCTTAAGT GGGGTCAAGC CTCTGACCCA CCACCCTGTT CTCTAGGGAG CACCTGCCTG 540
GGTCCCCGGA TTTGTCCTGT TGTCGCTTTG CAGCATGGCC CAAGGTTCTT CTGATGGAAG 600
CATGACCACC AGCCAGTGCC AAGTGGAGTG GGTCCTGGGG TGGGCGTGAA GAGCTGCTGC 660
CATCACCCCC AGAGCTGTAG ACAGGCGCTC CTGCACACGT CTGCTGGTGA CCAGTGCCAC 720
CTCCCTGTGC CTCACCACTT ACCCAAAATC CTGGCCGGGC TGGGTGGCTC ACACCTATAA 780
TCTCAGTACT ATAGGAGGCC AAGGCAGGAG GATCGCTTCA GGCCAGGAGT TCAAGACCAG 840
CCTGGGCAAC ATAGACCCTA TCTCTGCAAA AAAATTTAAA CATCAGCAGG GTGTGATGGC 900
GCATACCTGT AGTCCCAGCT ACTCAGGAGG CTGAGGTGGG AGGATCACTC AAGCCTGGGA 960
GGTCAGGGCT GCAGGGAGCT GTGGTTGCAC TCCCAGCTGG GTGACAAAGC AAGACCGTGT 1020
CTCAACAACA AAAAAAAGAT TTTGGAAAAA TGGCCTCGGT GTGCTGCAGC AAGGTAAGCT 1080
GGGACTCGCC TCGATGCTTC CCAGCTGGCC AGGGAAGCGG AACATCCGGG TGAGCAGAGC 1140
CCAAACTGGT TCTGAGGATC TAGGAACACT TCCCAGGGAG TGGGGCTTGA GTTGGTTCCT 1200
GAAGCGGCTC AGCACGGTGA CCCCTAGGTT GTCCTGGTGG TAGTTGTGAC CACAGGAACA 1260
GGCAAAGCTC CTCTGGAAAT TCTAAGTATG TGCAGGTCTT TGTAAGTTCT CACTGCAGGT 1320
CTGTGGCCCT CAGCACCCTG CAAGGAGAAC AGGGCTTTGT AAGGGCTCTG GAAAGATCAG 1380
GAACAGTCAG AACATGCTGG ACCAGGTGTT CACACATGAC GTCTTGCAGA TGGTTCCCTG 1440
GTTTTGTTCT GTTTCAGTTT TTAATTGTCC CATTTTCTAA AATTGGAAAA CAATTGTTGG 1500
AAGAAGCTCC ATGCAGTCTA GGCAGCATCT TGTGTGTTTA GATGAGACTT AGTGGGTCAG 1560
GACCGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT CGAACAGCAG 1620
AGTGACATCA GGTGACAGCC TTGGGTTAGC ATCACAGATG CAGCAGGCAT GGTGTGGTGT 1680
GGGTGAGCTG AAGGGAAATG CAAACCGTTT TTAGGACAAA GAGGCCTTGT TCTGGTCACT 1740
GGCGAGCAGC TTGGCCCTGA CTCACCCCTG AAGCTCCTGA ATTGTCGCCG TTGGGGCAGG 1800
GCAGACAGGG ACATAACCTA CCCAACATCA CTGCCAACAT CCTTGCGCTT TTCTGGATAT 1860
AAAAAAGGTA CTTCTGGATC CGAAATATCT AAGCTAGATG TGAGAGCGTC AGCTTGCTCC 1920
ACTGGGGAGG GAACTTCAGA GCCAGCCCCC CTCACCCAAG TACTACTGCT GGTGATGGCT 1980
GGGGTGGGTG AGGGTGAAAG AGGGGCATCA CCAGCCCCAT GAACTCAGTG TGGTCTGAGA 2040
GTGCCTTCTG GAGGGGGTGG GGGATGGGGG ATGGGGAATG ATAGGCTGAG 2090
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