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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS133-13328
Organism
Homo sapiens
Tissue/cell
melanoma
Coordinate
chr17:73809300-73809840
Target genes
Number: 38
Name
Ensembl ID
HN1
ENSG00000189159
SUMO2
ENSG00000188612
MRPS7
ENSG00000125445
AC011933.1
ENSG00000257073
AC011933.2
ENSG00000228007
GRB2
ENSG00000177885
TSEN54
ENSG00000182173
RECQL5
ENSG00000108469
SAP30BP
ENSG00000161526
ITGB4
ENSG00000132470
GALK1
ENSG00000108479
H3F3B
ENSG00000132475
UNK
ENSG00000132478
UNC13D
ENSG00000092929
WBP2
ENSG00000132471
TRIM47
ENSG00000132481
TRIM65
ENSG00000141569
MRPL38
ENSG00000204316
FBF1
ENSG00000188878
TEN1
ENSG00000257949
RP11
ENSG00000261408
ACOX1
ENSG00000161533
CDK3
ENSG00000250506
SRP68
ENSG00000167881
GALR2
ENSG00000182687
ZACN
ENSG00000186919
EXOC7
ENSG00000182473
ATF4P3
ENSG00000228218
RNF157
ENSG00000141576
FAM100B
ENSG00000185262
QRICH2
ENSG00000129646
SPHK1
ENSG00000176170
UBE2O
ENSG00000175931
RHBDF2
ENSG00000129667
PRCD
ENSG00000214140
JMJD6
ENSG00000070495
METTL23
ENSG00000181038
MFSD11
ENSG00000092931
TF binding sites/motifs
Number: 1
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
ZNF263
MA0528.1
chr17:73809323-73809344
GAGGGAGGAGTGGCAGGGAAG
+
6.18
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr17
73809406
73809470
Enhancer Sequence
AGGCCCCAGG AGGCCAGCCA CGGGAGGGAG GAGTGGCAGG GAAGGGGTCA GGCAGAGGCT 60
GCTCCCACTG GCTCTCCGGG AGGAGGGGAG GCTGGTCCTG GGGATGACAG GATCGCAAGC 120
CCAGGGCCCA GGGGAGGGCA TAGTGAGGAT AGCTGGACAG TAGGAGCCCA GCTTCACCTC 180
CTGCATGAAT GAGGACCCTG GTCAGACCGT CTCTGAGGCT CCACCGCTCC TGATCCTGAG 240
GGGAATGTGT TGAATGAGGA CCAGGCCACA GCGTGGACAG TGTGGTTGTA GCTCCAGCCT 300
GACCCTACTT GGGCTAGTGG GAGGGCCTGG CTGAGGGGAA TCAAACAGTA TCCTTTGTGG 360
TGATTCGGCC AGGCTGGGTC AGAGAAAGAG CTTGGCTTGT GGCACCAGCA AGGCCCTGAC 420
TCTGCAGCTG GTCTTTTCCA TTTCTGTGCT CATGCCTATG AGGCTGGGTC CAGGTGGCAC 480
CTGCTAGGCT CCGATCTCAC CTTCTCCTTT CTCCATCTGA CCCCACCCTC TTGTTGGCCA 540