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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS121-13167
Organism
Homo sapiens
Tissue/cell
LNCaP
Coordinate
chr16:719610-720120
Target genes
Number: 26
Name
Ensembl ID
JMJD8
ENSG00000161999
FAM195A
ENSG00000172366
RPUSD1
ENSG00000007376
STUB1
ENSG00000103266
HAGHL
ENSG00000103253
NARFL
ENSG00000103245
LA16c
ENSG00000262528
C16orf13
ENSG00000130731
RHBDL1
ENSG00000103269
WFIKKN1
ENSG00000127578
RAB40C
ENSG00000197562
PIGQ
ENSG00000007541
FAM173A
ENSG00000103254
METRN
ENSG00000103260
FBXL16
ENSG00000127585
Z98881.1
ENSG00000196674
CHTF18
ENSG00000127586
CCDC78
ENSG00000162004
WDR90
ENSG00000161996
WDR24
ENSG00000127580
NME4
ENSG00000103202
MRPL28
ENSG00000086504
RAB11FIP3
ENSG00000090565
AL022341.3
ENSG00000228201
AL022341.1
ENSG00000197727
RHOT2
ENSG00000140983
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3
Chromosome
Start
End
chr16
719974
720042
chr16
719733
719967
chr16
719637
719729
Enhancer Sequence
GCCCTCAGTG CAGACCCCAA CAGCAGAGAC ACAGTGGCCG GTGGTGGCCC AGGTGGACCT 60
TCACCCAACC CGTGGCCAGT GCCATCGCTC ACAGCATTTT GGGGAGCCTG ACGTGGAGTT 120
GCCTGACGTG GAGTCACCCG GCCCTCTCCT GTGATCCCAC TTCCCCTGAG AGGGTCTGGG 180
GCGTCCCGCA GTCTGAGCCA TTGAGGCCGG CAGTCCTCTT TCTTCCCCAG TTTCCAAACC 240
CCCGGGGGGG GACCCGCAGA GGGCCTGCGT TGGGGGCGGC CCTAGGCTTG GGCCCCAGTG 300
ACTTGGGGGT GTTTGGGAGC CATTGGGGTC AGACAGATGA GGCTGCACCT GCTGCCTGCC 360
TTCTCCCACC AGCTTTGTTC CTGTGGCCGG GACTTGGGCC CTCAGTGGGC CTTGACCTCC 420
CCCTTCTGCT CTCCCCCAGC CAGGCTCATG CTCCAGCTGG GAGCCATGTG CCCGCGGGCA 480
GCCTCACTTC ACAGCCAGGC TTTGCTTTTC 510