EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS091-23924 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:36266570-36268540 
Target genes
Number: 45             
NameEnsembl ID
HPNENSG00000105707
FXYD1ENSG00000221857
LSRENSG00000105699
USF2ENSG00000105698
HAMPENSG00000105697
CD22ENSG00000012124
AC002511.4ENSG00000205786
AC002511.3ENSG00000232680
FFAR2ENSG00000126262
KRTDAPENSG00000188508
DMKNENSG00000161249
SBSNENSG00000189001
GAPDHSENSG00000105679
AD000090.2ENSG00000236144
TMEM147ENSG00000105677
ATP4AENSG00000105675
HAUS5ENSG00000249115
AC002115.6ENSG00000089336
RBM42ENSG00000126254
ETV2ENSG00000105672
COX6B1ENSG00000126267
UPK1AENSG00000105668
AD000671.1ENSG00000239352
AC002314.3ENSG00000241762
ZBTB32ENSG00000011590
MLL4ENSG00000105663
IGFLR1ENSG00000126246
U2AF1L4ENSG00000161265
PSENENENSG00000205155
LIN37ENSG00000188223
HSPB6ENSG00000004776
C19orf55ENSG00000167595
ARHGAP33ENSG00000004777
AC002398.5ENSG00000225872
PRODH2ENSG00000250799
NPHS1ENSG00000161270
KIRREL2ENSG00000126259
APLP1ENSG00000105290
NFKBIDENSG00000167604
HCSTENSG00000126264
THAP8ENSG00000161277
WDR62ENSG00000075702
TBCBENSG00000105254
POLR2IENSG00000105258
ZNF146ENSG00000167635
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs231227chr1936268067hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXP1MA0481.2chr19:36268007-36268019AGGTAAACAGAA+6.14
GLI2MA0734.2chr19:36268359-36268374AGACCACACACGAAG+6.95
KLF16MA0741.1chr19:36266638-36266649GCCCCGCCCCC+6.02
KLF5MA0599.1chr19:36266624-36266634GCCCCGCCCC+6.02
KLF5MA0599.1chr19:36266638-36266648GCCCCGCCCC+6.02
PPARGMA0066.1chr19:36266775-36266795ATGGGGTGACAGGGACCTAG-6.31
ZNF263MA0528.1chr19:36267028-36267049CTTTTCTTCTCCTTCTCCCTC-6.05
ZNF263MA0528.1chr19:36267195-36267216TTGTCCTCATCCCCCTCCCCC-6
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr193626660036268309
Number: 1             
IDChromosomeStartEnd
GH19I035777chr193626824136268410
Enhancer Sequence
GGGTCCCACG CGGCCGTCAG CCTGTCCGTC CGGATGTCAG TCTGTCCGTG CGCAGCCCCG 60
CCCCGCGCGC CCCGCCCCCG GCCCCGCCCG ATCCCGCGGC CTGTGCTTCA GCCGTGGTCC 120
CTCCCGTCCT GCGGCCCCAT CCCGGGTCCC AGCCCGTACC TCGACCCCGC CCCCTAAGCG 180
CGCATCCCCG TCTTCCACGC CCTGGATGGG GTGACAGGGA CCTAGGGCCT GGGCTGGGAG 240
GAGGCGGGGC TAGTCCAGGA AGGGACCCGC GCCACCCAAG TGGCCCCTGC AGGGGCCTCC 300
TGAGGCTCCT GGGTCCTTCC CCAGCTCCCA TCCCAGCACC TTCCTCGGCA TCCTTCTGCC 360
AGCCCTCAGC CCTCCCCGGC GGAGCCCCCT CCTCCTCCCC ACAGCCCCTT TCTCATTCCC 420
GAGCCCCACC CCCCACCCGC TCCATCCCCA GCCTGACCCT TTTCTTCTCC TTCTCCCTCA 480
TTTTCACCCT ATCCCAGTTC CTCTCAATCC CCCCCGCCCC GCATCAGTCT GAGCCTTTGC 540
CTCGTCTCTC CAGCCACTCC TTCCTTACTC CACCCCAACA GGCCAGCACT GTACCTCCCT 600
TGATCCTCGG GTCTGCTCCA TCTCCTTGTC CTCATCCCCC TCCCCCACCA TTTCCCTCTC 660
CCACCATGCT GCTCCCGCTC ATTCATCCAT TCATTCCCTC ACTTAGCAGA CATTCACTGA 720
GACCGCCTCT GTGCAGGCCC CACGCTCCAG GCACAGAGAG AGTCAGCTCC CATCCTGCCT 780
TGGGGAACCT TATGGGCTGG AGGGGGACAG ACCCTGAGGG TGAGACCCTG AGGGTGACTG 840
GGGGTTGCAG GGACATGGAG CAGGGAGACG CTACAGCCCA GTGAATCTGT CTGGCAGCTG 900
GTTAATTTAT TCATCAGATT TTACCCAGTC CCTGCTGCGC GCGACTGGGC TGGCACTGGG 960
GACCCAGAAA AGAATCAGGA ACAATCATGT CTGAACACCA ACTCAATGCC CAGCTCTATG 1020
CTGGGGAGCT CAGTCTGGGG CCCTCCTTCT GGGAGGCCGG TCATAGTCCA ATGAGAGAGA 1080
TGAACTTGTC ACCACCAGTG CCATCTCAGA GTGATCAGAG CTGTGAAGGG AGAAGCTCTG 1140
GTCAAGGCAT GGAACCTGGG ATGGGGGAAC CTCAGGGGAT GGAGAGAGTC CAGAGGAGAT 1200
GCCAGGTGCA GCCTGAAGGG TCAGGGAGAA CTTCCTGGAG GAGGGCACAT GTGAGTTGGG 1260
ACCTGAGGGG TGGGAGTGAG GATGAATGTA CCCAGGGAAA GGTGGGGCGA GTGTTCCAGG 1320
CTGAGGGAAC AGCCTTTGCA AAGGCCTAGA AGGAAATGAG AAGAGGGTGC TTTTTTTGGA 1380
CTCTTAGAAG TTCAAGAGCT CTGAGAGTGG GGGCAATGGG AAGAGATGGG ACTGGAGAGG 1440
TAAACAGAAA TCAGCTCAGG GAAGTCTCGA TTATCAGACC AGAGAATTCA GACTTCGTCT 1500
TGAAGACAAC AGGGAGTCAT TGAAGGCCCA GGATCTATGG AGAAATAGAG CCAGATTTGT 1560
GTTTTCTGAA AACGATCCAG GCTATTGCGG AAAAGCTGGC AGGAGGGGAG AGGCTGGAAG 1620
CAGGAAGGCT GATGAGATGG GAGTTGTGAT TGTCTAGACA GTGGTAGGAG ATCACTGTAC 1680
TCTGCAGGGG CTACGGAAGG GTTTTCAGCA GGGAGAGATG GGACCAGCAT GCTCTCCATC 1740
CTGTTGCCCC GCCTCACGTC TGGCCCCTGC TTCTCCAGTC CCCCACCCCA GACCACACAC 1800
GAAGAAGCAG TCCTGTCCTC AGCCCAGCCC TCACCTCCCC CGACCTGCCA TCCTGCTTCA 1860
TGCTCAGGGC GGTGTGTGGA GCGCCCGGGG CTCTGGACCC GCGCTGCCAG ATAACAATGC 1920
TCTCGTTGTC TCTTTGCTCC CATCTCTGGG GGCCTCTGAT TCTTTCTGCT 1970