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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS133-32972
Organism
Homo sapiens
Tissue/cell
melanoma
Coordinate
chrX:153033370-153033700
Target genes
Number: 33
Name
Ensembl ID
HAUS7
ENSG00000213397
FAM58A
ENSG00000147382
RP11
ENSG00000260081
DUSP9
ENSG00000130829
RPL18AP16
ENSG00000237793
SLC6A8
ENSG00000130821
PNCK
ENSG00000130822
BCAP31
ENSG00000185825
ABCD1
ENSG00000101986
PLXNB3
ENSG00000198753
U52111.14
ENSG00000232725
SRPK3
ENSG00000184343
SSR4
ENSG00000180879
IDH3G
ENSG00000067829
PDZD4
ENSG00000067840
U52111.12
ENSG00000184844
L1CAM
ENSG00000198910
ARHGAP4
ENSG00000089820
NAA10
ENSG00000102030
RENBP
ENSG00000102032
HCFC1
ENSG00000172534
TMEM187
ENSG00000177854
IRAK1
ENSG00000184216
MECP2
ENSG00000169057
FLNA
ENSG00000196924
EMD
ENSG00000102119
RPL10
ENSG00000147403
DNASE1L1
ENSG00000013563
BX936347.1
ENSG00000197180
ATP6AP1
ENSG00000071553
GDI1
ENSG00000203879
FAM50A
ENSG00000071859
G6PD
ENSG00000160211
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chrX
153033391
153033445
Enhancer Sequence
GAGTGGCATG CCCTTCCATC CCCCCTCTCT GTGGATGGCT GGCATCTTTC AGCACTGGAC 60
AGGGGTGCCT GCCCATGGGA AGTGCCAGCC AACCTCTCAG CCAGGGGTCA GCTGAGTCTC 120
CAGGTCTCCT GCCTGCTCTC CACCCATTTC TTTCCACCTT TCTCCCTCTG GATGCTATGA 180
GCTTGCCAGG TGCCCTGGCC CTTCGGCCCT GATTGCTGGG CCTTGGGGTC ATCCCAGGGT 240
GCCTGGCTCT CCTCCCGCTG GCAGCCTGGG TACCCCCCCT GACTGCCTCT CTGCTCTCTT 300
CCGGGGGCTG ATTCTCCACT TCCTGCCACG 330