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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS091-34260
Organism
Homo sapiens
Tissue/cell
HepG2
Coordinate
chr3:50335100-50336250
Target genes
Number: 23
Name
Ensembl ID
MON1A
ENSG00000164077
RBM6
ENSG00000004534
RBM5
ENSG00000003756
SEMA3F
ENSG00000001617
RP11
ENSG00000235016
GNAT1
ENSG00000114349
SLC38A3
ENSG00000188338
GNAI2
ENSG00000114353
U73166.2
ENSG00000230454
U73167.7
ENSG00000232352
SEMA3B
ENSG00000012171
C3orf45
ENSG00000179564
IFRD2
ENSG00000214706
NAT6
ENSG00000243477
HYAL3
ENSG00000186792
HYAL1
ENSG00000114378
HYAL2
ENSG00000068001
TUSC2
ENSG00000114383
RASSF1
ENSG00000068028
ZMYND10
ENSG00000235058
CYB561D2
ENSG00000114395
NPRL2
ENSG00000114388
TMEM115
ENSG00000126062
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr3
50335695
50336071
Enhancer Sequence
CTCCTGTAGA TAACAGCCAT GCTGGGCTGT GCCAGGAGGG AGGGTGGGGT TGGAGCAGGG 60
AAGGGCTGAC AGAGTGCAGG GGGGACCATG CATACTGGAA CTGGGGAGTG GTGGGCTGCA 120
CTTTGTCCCA CACTCACCTG ATAGCACAGG TGACCTGGAA GAGACCCATC CCCTATAGAG 180
CAGGGCAGAT AGATCCAGGT GTCTACCCCA CATTGGAGGG AGGCTGGGAG TGATGGATGA 240
GCTGCTTAAG GCTGGGGCAG AACCTAGGAG TCCTGGCCCC AGCCTGCTCT GGCTACAAAT 300
TTGTCCTCCT CAGGACCTCC CCTCACAGGG GGTCTGTAAC CACCAGGTCT ATAAAACAGC 360
CGACCCAATC TACTTGCTGG CCTTCTGTCT TCCAGTAGTC CTCCTAGTCC ACCACTAGGG 420
CATGGGATAG AAGATGCAAA GCAGACACTA TACCCCCTGC TCAAACCTAC CCAAGGTTCC 480
CTCCATAGGA AAAACTGCCC GGGAGTCTTC CTGTCCCTTT CTTCTCCCTA TGTTCCGAGT 540
CTCCTCCAGC TCCCAGCCTT TTCAACTACC TGGGCTATGC CCACTGCCTT AGTGGATCCT 600
GGGGCCCCAC TCATGCACCC ATCAGGCTGA GCTTTGGCCT GTCTTGACTG CCTTCCCCAC 660
CTGGAGCCCA TGGCCCCCTT CCCAACTCTG CCCATCTCAG GACACTTTGG ATATAGACCC 720
AACTGTCTCC TCAGATGGGG CCCCAGCAGC ACCAGCACTG GGCCTGGCCC ACAGTCACAC 780
AGCAGTATTG CCTCTGCAGG CTTGGTTCCC CACTGGCTTG AGTTTCGCAG GCACCCTAGA 840
TAAGGACCAC AGCTTCCTTC CTATATCCAC AGGGTGTCCA ACGGTCACCA GGTTGGGGGC 900
CCAGACCTCC TGTGCCCAAA CCCTACTGTT TTCCCATCTT AACCAAGGTC CTGCCGTCCG 960
GCAGGTCTAT GCTGGGGGTT TTCTAGTCGT GGGCGGGCAG CTGAGCCCCC TCCTTCTACT 1020
CACCTGCTCC AGAGGGGGCC TCCTGGCTCC CCTTACCTCT CCTGAGCTTG AGGCCAATTA 1080
AACACTGGTC AGTAACAGGC ACCCCCCTCC CCTCACCTCC CACACCATTC ACAGGGCTGT 1140
AAGCCCCTCA 1150