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

TagContent
EnhancerAtlas ID
HS091-22738 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:1395590-1397020 
Target genes
Number: 47             
NameEnsembl ID
WDR18ENSG00000065268
PALMENSG00000099864
C19orf21ENSG00000099812
AC004449.6ENSG00000261204
AC112708.1ENSG00000213726
ARID3AENSG00000116017
KISS1RENSG00000116014
R3HDM4ENSG00000198858
MED16ENSG00000175221
PTBP1ENSG00000011304
CFDENSG00000197766
GZMMENSG00000197540
MADCAM1ENSG00000099866
TPGS1ENSG00000141933
GRIN3BENSG00000116032
C19orf6ENSG00000182087
CNN2ENSG00000064666
ABCA7ENSG00000064687
HMHA1ENSG00000180448
POLR2EENSG00000099817
GPX4ENSG00000167468
SBNO2ENSG00000064932
STK11ENSG00000118046
C19orf26ENSG00000099625
ATP5DENSG00000099624
MIDNENSG00000167470
CIRBPENSG00000099622
C19orf24ENSG00000228300
MUM1ENSG00000160953
EFNA2ENSG00000099617
AC005330.1ENSG00000240846
NDUFS7ENSG00000115286
GAMTENSG00000130005
DAZAP1ENSG00000071626
RPS15ENSG00000115268
APC2ENSG00000115266
C19orf25ENSG00000119559
PCSK4ENSG00000115257
REEP6ENSG00000115255
ADAMTSL5ENSG00000185761
PLK5ENSG00000185988
AC027307.1ENSG00000222720
MEX3DENSG00000181588
MBD3ENSG00000071655
U6ENSG00000252933
TCF3ENSG00000071564
KLF16ENSG00000129911
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GLIS2MA0736.1chr19:1395633-1395647GACCCCCTGCGGCG+6.07
KLF16MA0741.1chr19:1396969-1396980GGGGGCGGGGC-6.02
KLF5MA0599.1chr19:1396970-1396980GGGGCGGGGC-6.02
RORA(var.2)MA0072.1chr19:1396857-1396871CTGACCTAGTTACC-6.02
SP2MA0516.2chr19:1396967-1396984GGGGGGGCGGGGCGGAT-6.2
SP3MA0746.2chr19:1396968-1396981GGGGGGCGGGGCG-6.11
TFAP2CMA0524.2chr19:1395832-1395844TGCCCTAAGGCA-6.04
TFAP2CMA0524.2chr19:1395832-1395844TGCCCTAAGGCA+6.32
ZEB1MA0103.3chr19:1396618-1396629GGGCAGGTGGG-6.14
ZIC1MA0696.1chr19:1395633-1395647GACCCCCTGCGGCG+6.78
ZIC3MA0697.1chr19:1395633-1395648GACCCCCTGCGGCGT+7.07
ZIC4MA0751.1chr19:1395633-1395648GACCCCCTGCGGCGT+6.8
ZNF740MA0753.2chr19:1396964-1396977GTGGGGGGGGCGG-7.82
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_06415chr19:1377850-1398313Brain_Hippocampus_Middle
SE_31970chr19:1394663-1395876Gastric
SE_34574chr19:1395349-1396847HCT-116
SE_41646chr19:1394184-1397285LNCaP
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1913957081396605
Number: 1             
IDChromosomeStartEnd
GH19I001395chr1913953501396847
Enhancer Sequence
GTGGTGTGTG GGTGAAAGGA GCCGGGGACG TGGGGGGATC ACAGACCCCC TGCGGCGTGC 60
CGCCCTTGGG CTGGGGGCGG TTGGAGCAGA GCCGGGGGCA GAGACGGGCA CTGTGCCTGC 120
CAGCAGGGTC CTTTCCCGCT GCTCTGCGAA GACCCTGGGG TGGACATCGT GGCCCAAAGT 180
CCCGAGCGTG GAAGGCCGCA CACCCATCCT TCCTGGGAGG GCCCTGACTC AGTCTCCCTC 240
TATGCCCTAA GGCAGGCTGA GCAAAGCCCG TCTGAGCCTG CCCCGGGGTT CAGAGTGTGG 300
CCTGTGGCCT GCGTGTGGAC TTGGGCAGGT CGCCACTGCC CTCTGGCCCA TTTCCAGGCG 360
GTGGCATGGG CTGGTTAGCT GAGGGCTGGG GCCAGGGAGA TGGGGAGGTG GCACCTGGTC 420
CAAACCAAAG GGCTGCAGGG CAGGACTGTG AGCCTCACAG GCTGTCTGAC CCCACTTTGG 480
GGACCCTCTC CACCCAGGGC TTTCGGGGAA CCCTGACTCC ACCCCACCAG CCCCTTCATC 540
CGTCGAAGTC CAGGCCTCAT CAGGGACGTG CATTCATTCA GCAAACGTCC CATCTTCCTG 600
TGTTCAGCGC CAGATGCCGC CGGTGCTGGG ACCTCGCTCT GCAGGCCCAC CCTGCATGCC 660
TGCTGCACAC CAGGGACAGT TCTGGGGATC GGCAGTTATG ACGGGCCAGG CTGGGATGGG 720
GCCCGGGAGA CTGGGGCGGG GGTGGGGAAG AGGCACCCAG CCCAGCCGGG TCAAGCAGCC 780
TGGAAGCAGG ACATGCTGGG GTGGGGACAG GGCGTCAGCC AGCGGAACAG CAGCCCTGGG 840
CCAGAGTGCA GAGCACAGGA GCCGGCCTTC TCTCAGGGCA AGGAGGTCAG TGGAGGGGGC 900
GAGCAGGACG GCCCCAGGAA GATGGGCGGG CTGCACACAT GTGGATGCAG GGGGCAAAGT 960
GGGAGGCATG GGGTGACCAG CTGGGCACAA GGGCACAGAC AGGCAGGACC CGGGATGTTC 1020
CTGGGGCTGG GCAGGTGGGG CTGCCCCTGC AATGGGCCCA GCAGGGGCGA TGCCTCCTGA 1080
GAGGAAACCA CATCTGGAAA TGGGAGGCTT GGGGAACGGG GCTGTCAGCA GCCACGCCCC 1140
TCCTGGGGCG GGAGGAGGGG AGCTCAGGGT GTGCTGGGGC GGGCAGAGAA GTGGGTTCCT 1200
GCCTGGGGTG GGCAAAGATC CTTGTCCCAC CCACACCCCG GCCGTGGTGC TGCCACCCCC 1260
TGAGACCCTG ACCTAGTTAC CCCCTTCCCT GACCCCACTG CAAAGGGTCA GGTGGCTTTC 1320
ATCTGAGGAA GGGACATCGG GCATCAGCTG GAGATGTCTG CTATGGGCAA GACAGTGGGG 1380
GGGGCGGGGC GGATCCTGGG GCCGCTCAGA AACCTGGAGG GGAGTCACCC 1430