EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS092-08233 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr11:876260-878070 
Target genes
Number: 44             
NameEnsembl ID
HRASENSG00000174775
DRD4ENSG00000069696
ANO9ENSG00000185101
TSPAN4ENSG00000214063
PTDSS2ENSG00000174915
POLR2LENSG00000177700
RNH1ENSG00000023191
DEAF1ENSG00000177030
CD151ENSG00000177697
EFCAB4AENSG00000177685
SIGIRRENSG00000185187
LRRC56ENSG00000161328
PNPLA2ENSG00000177666
C11orf35ENSG00000185522
RPLP2ENSG00000177600
PIDDENSG00000177595
RASSF7ENSG00000099849
PHRF1ENSG00000070047
IRF7ENSG00000185507
PSMD13ENSG00000185627
AP2A2ENSG00000183020
CHID1ENSG00000177830
ATHL1ENSG00000142102
IFITM2ENSG00000185201
IFITM1ENSG00000185885
IFITM3ENSG00000142089
B4GALNT4ENSG00000182272
PKP3ENSG00000184363
AP006621.1ENSG00000177236
TALDO1ENSG00000177156
RP13ENSG00000254739
RP11ENSG00000254815
MIR210HGENSG00000247095
SIRT3ENSG00000142082
AP006621.6ENSG00000255142
TMEM80ENSG00000177042
EPS8L2ENSG00000177106
AP006621.8ENSG00000255108
CDHR5ENSG00000099834
SLC25A22ENSG00000177542
CEND1ENSG00000184524
AP006621.5ENSG00000255284
PDDC1ENSG00000177225
TOLLIPENSG00000078902
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11876502877035
Number: 2             
IDChromosomeStartEnd
GH11I000878chr11876261876790
GH11I000877chr11877781877930
Enhancer Sequence
CCCTGTGCAC GTTGCAGGCA GTGAGCCCTT GGGCTGGATT TGGTGTCCAG AGTGGATGAC 60
ACCTGTCCAG GGCAGGACCA CAGGGTGCAG ATGAACAGTG CAGCTGAGAG GGAGGTCGGG 120
GCTCAGGGAG GGGCTGGACA CCACCTGGGC AGAGCCAGGG TCAGGAAGAA TGTTCCAAGG 180
AGCTGCGAAC ACGGCCCCTC CACCGTGCAG ACATTCAGGC GGAGGCAGGA GTGCCGTCCA 240
CTCGTAGACG GGACTCTGGC ACAGTTGAGA GCCAGGAACC TACCCAGGGA AGACACTGGT 300
GGCTGTCAGG CATCACACTC CCAGCAGCAG GGTTGCCTCT GCCTGTGATC CTTGCCAGTG 360
TCCTCCTTGG ACTAGAGTGG GCGTGCCCTC CCTGCTGTAC CCTTGAGGCA GGAGCCATGG 420
CTGTGCAGCG TCAGCACTCT CTCGGCCGGC TCGGCAGCTG TGAGGATGCA CGTGTGAGCG 480
AGTCTTGGCA GCCGTTTATT TATTCCAGCC TTGCGGGAGG TGGCCCTGCT GAGCTGGCAT 540
CTGTGCCGCT GCCCTGGCCA AGGTCTCTAG GCAGGGACAG ACAGGGCAAG AGCTACTGGC 600
CACCCAGGAT GGGACGTGGG GACGGGCACT CTAGGGGCCC CTGAGACCCA GATCTCCCTA 660
TGGCCTGCTC CCCTCCAGTG GTCCTGCATC CAGGCTGGAG CCTGCCAGGT GCCCACACCC 720
CTCCTCTGTG CCACTCAGGC CCAGAGGTCA TTAACAAGGG CACTTCGGGT GGGCGAGGAG 780
GGCAGATGAG GGGACTTCTC AGCTGGGAGT GAGGACCCAG AAGCAGTGCC TTTCTTTCCT 840
GACTGGGTGC ACACAGACCC CAACTTGTGC AAAGCTGGGG GGTCCTGAGG GCATACACCC 900
CCACACGCTC ACATACACAC CTTTGTAATC AGAATTCCTT GGCCCCAAAC CCCCTAGCCA 960
ATTCTCAGAA CAATCATGGG TGGGTGCAAC TGCCCACGGG AAGCTGCTGA AGGCTTTGGT 1020
TGTTTTGGAG ACAGGGTCTT GCTCTGGAGC CCAGACTGGA GTGCAGTGCA GTCTCCACCT 1080
CCACAGCTCA GGCATTCCTC AGCCTCCTGA GTGGCTGGGA CCACAGGTGT GCACCACCAT 1140
ACCGGCTAAT TTGTTTTTAA ACTATTTGTA ATGATGGGGT CTCTCTATTT TGCATAGAAG 1200
ATCTCGAACC CCTGGGCTCA AGCAATCCTC CTGCCTTAGC CCCACAAAGT GCTGGGATTA 1260
CAGGTGTGAG CTGTTGCGCC AAGCCACACT GATGCCTTGT GTGACCTGAC CCAGGCTCTT 1320
GTGCAGTGAG TGAGCCCTAA CTCATCACCC TCAGATGGTG TAATGGGCTG AGCTGTTCCC 1380
CTAAAATCCA CAGGGTGAAG TGTGTGATGT CTTGAATGTT CTCTGCAAAA TTCACACTGA 1440
AATGTAATAC CCACTGTGGC ACTGTGGGGA GGCGGGGCCT TTAGAAGGCG GCACTGTGGG 1500
GAGGCGGGGC CTTTAGAAGG CGGCACTGTG GGGAGGCGGG GCCTTTAGAA GGCGACACTG 1560
TGGGGAGGCG GGGCCTTTAG AAGGCGGCAC TGTGGGGAGG CGGGGCCTTT AGAAGGTGAC 1620
TGGGTCATGA GGGCTCCGCC CTGGTGAACG GATTAATCCA TTCATGGACT AGTGGGTTAA 1680
TGGACCAGTG GGTGACCATG GGCATGGGAC TGTGGCTTTC TAAGAAGGGG AAGGCGGCAG 1740
CTCGCTCAGA CCCTGTACCA CGGACACCCT GCACCACCTC CGGACTCTTC GGAGTCCCTA 1800
CCAGCAAGAA 1810