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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS133-00852
Organism
Homo sapiens
Tissue/cell
melanoma
Coordinate
chr1:27286070-27286840
Target genes
Number: 30
Name
Ensembl ID
PAFAH2
ENSG00000158006
EXTL1
ENSG00000158008
UBXN11
ENSG00000158062
DHDDS
ENSG00000117682
RP3
ENSG00000223583
HMGN2
ENSG00000198830
RPS6KA1
ENSG00000117676
RP5
ENSG00000260063
ARID1A
ENSG00000117713
PIGV
ENSG00000060642
ZDHHC18
ENSG00000204160
RP1
ENSG00000226698
GPN2
ENSG00000142751
NUDC
ENSG00000090273
GPATCH3
ENSG00000198746
OSTCP2
ENSG00000225294
TRNP1
ENSG00000253368
FAM46B
ENSG00000158246
SLC9A1
ENSG00000090020
RP11
ENSG00000229985
WDTC1
ENSG00000142784
TMEM222
ENSG00000186501
SYTL1
ENSG00000142765
MAP3K6
ENSG00000142733
GPR3
ENSG00000181773
WASF2
ENSG00000158195
AHDC1
ENSG00000126705
FAM76A
ENSG00000009780
STX12
ENSG00000117758
XKR8
ENSG00000158156
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr1
27286400
27286800
Enhancer Sequence
TAAGGCACCG CAAGGATGTT CCCGGGGGTC AGAGGGTCCC GGCCCGCCCT CCCTGGATTT 60
CTCGTTGATG CTTTCCTCTT CCCCCTTAGT CCCGCGAACA CACACACACA CTCAAGGGTC 120
TATGTACCGT CCCCTCCTCC GAGGGTCCCC AGGACAGGCC CGGCCGCACC AGCCTCTGCC 180
CCCAGCCCAG TGCCAAGCCT CGGACACCCG GCCGGGGAGG ACCACCCCAG TCCTGCTCGA 240
GAAACAGCCG TCGGCTCAGT GCACCCTCGG CCTCCTGCCC CAAAGGTGCA GCCCGAGAGT 300
CCCATATCCG CGGGCAGCTA GTCCTGGGGA CAAGGAAGAA CCAGATCCTG GCACTGTCCC 360
CCGGGCTACC ACAGCCCCTA CACCAACTCT GCCCTCGGGG CGAGCACTAC CCTCTCCAGC 420
TGCAAGGGCC CTACCCCGCG GGCGGACCCA GCCTCCCTCC CGTCCCGACG CTGTTCCTCG 480
GGGTGAGCAC CAGCGTTTGT CCCATCCCGA CGCTGCCCCC CGGTGAGTGC GGCCCCCGCA 540
CCCAGCCAGT GCAGCCCTAA GGGCGAACGC GGCCCCTCAC CCCATTCTGC GCGCCCAGCC 600
CGGGCGCCCG CTCAGGCCGC TCCCCAGCCC GGCCCGCGCA CCCCGGAAGT AGGAGGGTGG 660
CCCCCGAGGA ACCGGGCCCG GGACCCTCTC CTGTCCGGGC TCAGCTTCGG GGGGCTCCCG 720
ACACCGGCGC CGCCCTGGCT TGCGCCCCCC TGGGCCCGCG CCGGGCTTAC 770