EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-15930 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr16:745920-746770 
Target genes
Number: 44             
NameEnsembl ID
Z97634.5ENSG00000236829
Z97634.3ENSG00000241145
AL049542.1ENSG00000256323
LA16cENSG00000261691
JMJD8ENSG00000161999
MSLNENSG00000102854
FAM195AENSG00000172366
RPUSD1ENSG00000007376
STUB1ENSG00000103266
HAGHLENSG00000103253
NARFLENSG00000103245
C16orf13ENSG00000130731
RHBDL1ENSG00000103269
WFIKKN1ENSG00000127578
RAB40CENSG00000197562
NHLRC4ENSG00000257108
PIGQENSG00000007541
ITFG3ENSG00000167930
FAM173AENSG00000103254
METRNENSG00000103260
FBXL16ENSG00000127585
CHTF18ENSG00000127586
CCDC78ENSG00000162004
WDR90ENSG00000161996
WDR24ENSG00000127580
NME4ENSG00000103202
TMEM8AENSG00000129925
MRPL28ENSG00000086504
AXIN1ENSG00000103126
PDIA2ENSG00000185615
ARHGDIGENSG00000242173
RGS11ENSG00000076344
RAB11FIP3ENSG00000090565
DECR2ENSG00000242612
AL022341.3ENSG00000228201
AL022341.1ENSG00000197727
SNRNP25ENSG00000161981
POLR3KENSG00000161980
MPGENSG00000103152
RHOT2ENSG00000140983
SOLHENSG00000103326
C16orf11ENSG00000161992
LMF1ENSG00000103227
SOX8ENSG00000005513
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11861214chr16746611hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
YY1MA0095.2chr16:746588-746600GCTGCCATCTTG-6.32
Number: 1             
IDChromosomeStartEnd
GH16I000693chr16743207746530
Enhancer Sequence
AACCTGCAGG CGGGCGGGCG CCGGGTCAGG ATTGCAGGAG AAGGGGTGGA GCCCGCAGGG 60
AGGAAGCAGT AGGGTGTAAA CATGCAGGGA GCTGAACCCT GAAAACATTT GGCAGTGTGT 120
GAGGAGGCGG GGCATCGGGA CGAGAGCCCA GGGCCTGGCC AGGGCAGGTG CTGGGGGCGT 180
TGGCACCAGC GTTACAATTA GACTCCAGAC CCGGCTGCCA GGCGGCTCCT CTGACCTCTA 240
CTCCTGGGGG ATCCTTTCCC AGCTGCCCCT CAGCTCCCCC TCGCATCCTC CCCACACTGC 300
ATTTGTATTT ATTTATTTAT TTATTTATTC ATTCATTCAT TCAATCATTT TGAGACAGAG 360
CCTTACTCTG TTGCCCAGGT CCCAGGCTGG AGTGCAGTGG CATGATCTCA GCTCACTGTA 420
CCCCCCGCCT CCCGGGTTCA AGCGATTCTC CTGCCTCAGT GTCCTCCCAA GTAGCTGGGA 480
CTACAGGTGC CCACCACCAG GCCTGGCTAA TTTCTGCATT TTTAATAGAA ATAGAGTTTC 540
ACCATGTTGA CCAGGCTGGT CATGAACGCC TAACCTCAAG TGAGTGGCCT GCCTCGGCCT 600
CCCATAGTGC CGGGATGACA GGCTTGAGCC ACCGGGCCTG GGCCCTGCAT TTAATCCACT 660
GCCCTGCTGC TGCCATCTTG AAAATCTTGA GTGTCTTTGA ACAAGGGACC CACATTTTCG 720
CTTTGCGCGA GGTCCCCTGT AGTCAGTCCT TCTTTCCTCC CACCCCAAAG CCACCATCCG 780
CTCCCACCTC CATAGGGTTG CTGCTGCCCG CCCCTGCCCC CCAGCCCTGT CCCCCCCGAG 840
CCTGGTGCAC 850