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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS184-30607
Organism
Homo sapiens
Tissue/cell
T47D
Coordinate
chr8:145955200-145955840
Target genes
Number: 21
Name
Ensembl ID
GS1
ENSG00000214597
MIR939
ENSG00000216133
MIR1234
ENSG00000221802
CPSF1
ENSG00000071894
VPS28
ENSG00000160948
CTD
ENSG00000261139
GPT
ENSG00000167701
MFSD3
ENSG00000167700
RECQL4
ENSG00000160957
LRRC14
ENSG00000160959
C8orf82
ENSG00000213563
ARHGAP39
ENSG00000147799
ZNF251
ENSG00000198169
AF235103.1
ENSG00000244307
ZNF34
ENSG00000196378
RPL8
ENSG00000161016
ZNF517
ENSG00000197363
ZNF7
ENSG00000147789
COMMD5
ENSG00000170619
ZNF250
ENSG00000196150
ZNF252
ENSG00000196922
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr8
145955342
145955719
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH08I144730
chr8
145955385
145955586
Enhancer Sequence
GCACCTCCGC ACTCCAGCCT GGGCAGCAGA GTGAGACCCT GTCTCTGAAG AACCAAAACC 60
AAAACAGATC TCTCATCAGG CTATCAACAG GTTACATGTG TTTTTTGTGA CTACTCAGAT 120
AAAGATGTTC AATTGTAACA GTTTCTCAAC ATTGCAGGCA GGGCTGAGCC CACCCAGGGC 180
TGGCGTTGTT CCCAGGAGCG GGTGCCCTCA CCCACCAACT CGAGGCCGCT CACTCACTGT 240
GCAGCTGTAT GGCAGGCCCA GCAGTGCCTC TCCCTTCGTA CATCACCAGA GTCGGCTGAA 300
AAGTGCCAAA AGAGAACTCA GGAACCAAAC AGGGAAGTGG AGAGCCATGT TTTATCCACC 360
GGGCCTAAAG CCCCTCCAGG CGCGGGGCCC AGAGCGCCAA TCCCTGGACT GAAAGAGCAG 420
CAAGGGTGGG CTCTGCTGCC GCCCAGAGGC CTTCCGTGGT AAGACAGCCA CGGAAAGCAC 480
AGCGCGTGCC GCTGCGACGG GGCGTCCCGG GGGTGACACT GGCATGTGAC GCTGCGACGG 540
GGCGTCCCGG GGGTGACACT GGCATGTGAC GCTGCGACGG GGCGTCCCGG GGGTGACACT 600
GGCATGTGAC GCTGCGACGG GGCGTCCCGG GGGTGACACT 640