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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-19836
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr17:41367960-41368460
Target genes
Number: 33
Name
Ensembl ID
NAGLU
ENSG00000108784
COASY
ENSG00000068120
MLX
ENSG00000108788
TUBG1
ENSG00000131462
FAM134C
ENSG00000141699
TUBG2
ENSG00000037042
EZH1
ENSG00000108799
HMGN2P42
ENSG00000214578
RAMP2
ENSG00000131477
VPS25
ENSG00000131475
WNK4
ENSG00000126562
CCDC56
ENSG00000183978
CNTD1
ENSG00000176563
BECN1
ENSG00000126581
PSME3
ENSG00000131467
AOC2
ENSG00000131480
AOC3
ENSG00000131471
RP11
ENSG00000260105
AC100793.2
ENSG00000213373
G6PC
ENSG00000131482
SNORA40
ENSG00000212149
AARSD1
ENSG00000108825
RUNDC1
ENSG00000198863
RPL27
ENSG00000131469
IFI35
ENSG00000068079
VAT1
ENSG00000108828
CTD
ENSG00000240828
NBR2
ENSG00000198496
BRCA1
ENSG00000012048
NBR1
ENSG00000188554
TMEM106A
ENSG00000184988
ARL4D
ENSG00000175906
ETV4
ENSG00000175832
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr17
41368049
41368089
GeneHancer
Number: 1
ID
Chromosome
Start
End
GH17I043215
chr17
41367482
41371420
Enhancer Sequence
GTGGGTGGGT GCCCTTGGCT CCAAACCCCC CTTCCTAGCA ATACTTCGCT GTAACCTTTG 60
TCCAGTGTTA TGACCCTGGG CATGGGAAGC CAGAGATCTT ATGGCACCCA GAGGGTGTTG 120
GGAGCCTGAA GAGAAGTAGG AGCAACCATG AGCTCCATGA CAGATGGTAA GGATTGGGAC 180
TCTACACAGT AAGGGGTCAG AATCCGGGCC AGATAAGTAA ACCACAGGGG TGGAGTGGGG 240
TGACAGTGCC TGAGACTCTC TGGATGGACA GGACTGAATG GAAAGAAGCT GTACAGGATG 300
GACCTGGATC CTGAGGCAGC TTAACTTCGT AAAGTTGACC CCTCACCATT CAATGCCCCT 360
CCAAGGGGCT CCCAGTTTTC ATCCTCTGCA CCTGAAGCTT GTCATGGTAG ATGGGGCTCA 420
GGCCAGACAG CCAGGCTTTT GCAACTGTTT GGCTTTTCCT AAGGATGGGC CATCTTCACT 480
CCTCCCTTCC CTTGTCTTCA 500