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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS133-00767
Organism
Homo sapiens
Tissue/cell
melanoma
Coordinate
chr1:26135640-26136170
Target genes
Number: 28
Name
Ensembl ID
SYF2
ENSG00000117614
RP3
ENSG00000261349
RHD
ENSG00000187010
SDHDP6
ENSG00000224183
RP11
ENSG00000259984
TMEM50A
ENSG00000183726
C1orf63
ENSG00000117616
SDHDP1
ENSG00000238084
RHCE
ENSG00000188672
TMEM57
ENSG00000204178
LDLRAP1
ENSG00000157978
MAN1C1
ENSG00000117643
SEPN1
ENSG00000162430
RP1
ENSG00000255054
FAM54B
ENSG00000117640
AL020996.1
ENSG00000223474
STMN1
ENSG00000117632
PAFAH2
ENSG00000158006
EXTL1
ENSG00000158008
SLC30A2
ENSG00000158014
TRIM63
ENSG00000158022
PDIK1L
ENSG00000175087
FAM110D
ENSG00000197245
ZNF593
ENSG00000142684
CEP85
ENSG00000130695
SH3BGRL3
ENSG00000142669
UBXN11
ENSG00000158062
DHDDS
ENSG00000117682
dbSUPER
Number of super-enhancer constituents: 2
ID
Coordinate
Tissue/cell
SE_08467
chr1:26131188-26137945
Brain_Inferior_Temporal_Lobe
SE_65420
chr1:26135604-26138185
Pancreatic_islets
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr1
26135667
26135977
Enhancer Sequence
GGTGAGTGGG CCACACTGGC TGGCCTGGAG CACCGGGGAG GCATGACGGT ACAGCGCCCA 60
GAGGGGAGGG CCCAGCTTGA GCCCCCCAGC TCCACCTCTC CTCCCACTGC CGTCTTGGGC 120
AAGCAGCTTT GGCTCTCTGA GCCTCAGTTT TCTCACCTGT GGATCCGGGT GCTGATGACT 180
TCCTCGTAAG GCACGTGAGG GTTCAGAAAG AAAAGTTGTG GAACTTGCTT GGCACGGGGC 240
TGGTAGCCAT GGTTGTGCCA TCCACACAGA AGTGGGAAGG ACACCCAGTC ACACATGCCC 300
TCCAGAAGCT GTGAAGGCTG GGGGAGGGGG TCCAGGCAGG GCTTCCAGAG GAGGGGCATG 360
TGACCCGGGC CTCGAAGGAT GAGCAGCATT TGGAGAGCCT CGCTGCTGCC CACTGGCCCA 420
TCCACCTCCA CCCCCACACT CAGCCTCCTC TCCCTGATGA TTCTGGCCAA GGCTTCCCGG 480
GCTCCTGGGG AGAAGGTGGG CAGCTCTGGT GCAGCAGATC CCCTTCCCCA 530