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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS121-05912
Organism
Homo sapiens
Tissue/cell
LNCaP
Coordinate
chr11:864510-865510
Target genes
Number: 41
Name
Ensembl ID
HRAS
ENSG00000174775
ANO9
ENSG00000185101
TSPAN4
ENSG00000214063
PTDSS2
ENSG00000174915
POLR2L
ENSG00000177700
RNH1
ENSG00000023191
DEAF1
ENSG00000177030
CD151
ENSG00000177697
EFCAB4A
ENSG00000177685
LRRC56
ENSG00000161328
PNPLA2
ENSG00000177666
C11orf35
ENSG00000185522
RPLP2
ENSG00000177600
PIDD
ENSG00000177595
RASSF7
ENSG00000099849
PHRF1
ENSG00000070047
IRF7
ENSG00000185507
AP2A2
ENSG00000183020
CHID1
ENSG00000177830
IFITM2
ENSG00000185201
IFITM1
ENSG00000185885
IFITM3
ENSG00000142089
B4GALNT4
ENSG00000182272
PKP3
ENSG00000184363
AP006621.1
ENSG00000177236
TALDO1
ENSG00000177156
RP13
ENSG00000254739
RP11
ENSG00000254815
MIR210HG
ENSG00000247095
SIRT3
ENSG00000142082
AP006621.6
ENSG00000255142
TMEM80
ENSG00000177042
EPS8L2
ENSG00000177106
AP006621.8
ENSG00000255108
AC138230.1
ENSG00000243562
CDHR5
ENSG00000099834
SLC25A22
ENSG00000177542
CEND1
ENSG00000184524
AP006621.5
ENSG00000255284
PDDC1
ENSG00000177225
MUC6
ENSG00000184956
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr11
865173
865374
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH11I000861
chr11
861850
864921
Enhancer Sequence
GGTACGGCTG CCTTGGCCGC AGGCCCAACT GCAGGGCTGG GGGCTCCATC CTCACTCCCA 60
GGGAGCACTG TGGGCCCGGT GTGGACAGAG TGGCCCTGCA TGTGCCCTCA CGGGCAGCCA 120
GGACAGCGGG TGTGGATTTA CCAGGCCTGG AGGGGCAGCG CCAGCGACCC TGGGAGGCTG 180
TGCTGTGGCT CTATAGCGAC TGGGGCACAA GGGCACTGCT ACCCCACCCG GAGGGTGCGC 240
CCCAGGTTGT CCCCCGCCCT CTGACGCAGC GTCCTGAGCC GTCTGCTCCC AGCGCCCCAT 300
CCGGGCCGCG CACCGTGGGG TTCTCCTCTG TAGAGCGGCC TCTTCTTGGT CACTCACTCA 360
TATATTCAGC CATTTGTTTA TACTGGGATG AAGTCCTGGC TATTGAGGTT GCACTCCGAG 420
CTAGAACACA CTACTTTGTT TTGTGAATCA CACTGTCCGT CCTTGGCCCT GGGGAGCTTC 480
TGCCGTCTGC TGCTGGGTCC CCTGACGTGC CCCCATCAAC AGACTTTTCA TTTTGGGGCA 540
CGTCCTGACT TCCTGGCACT GCAGGGCGCT CCAGGCTCCT TCATTCCCTG CCCTGGCCCA 600
GGAATCAGCC CCTTCTCCAG GGTGCTCTGG GTCCTCACTG AATATTGGGG ACCGAGGCCA 660
GGGTGCTGGG TGGGCTCAGC GCTCATAGCC CCTGGCTTTC AGCTCACAGA GCATGGCTGC 720
ACGTGTCCCG ATACGTGGAG GCACCTGTGT CCCTGTCCTC TGTCCCCCCA GGACCCATGG 780
TCCTCCCCCA GCCTGGGGAG GAAGCCCAGA GGTGGGGGCC CTGGGCCTCA GGGCTGCTGG 840
GAGGACATGG GGCCGGTGTG TCTGCAGCTT GGTGGGCTAG GAGGCGCGGG GGACACAAGA 900
CCAGGCGCAG GAGGGGCCCA GCTTAGGGGC CGGCGAGGGG GTCTGGATGA GGGAGGCGGG 960
GTACAGTGGG AGGGGCCCTG CTGACCCCCC CCGCACCCCC 1000