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

TagContent
EnhancerAtlas ID
HS091-21582 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:79952760-79953860 
Target genes
Number: 57             
NameEnsembl ID
RP11ENSG00000262877
BAHCC1ENSG00000171282
RP13ENSG00000229848
ACTG1ENSG00000184009
FSCN2ENSG00000186765
C17orf70ENSG00000185504
YENSG00000207021
TSPAN10ENSG00000182612
NPLOC4ENSG00000182446
PDE6GENSG00000185527
CCDC137ENSG00000185298
C17orf90ENSG00000204237
HGSENSG00000185359
ARL16ENSG00000214087
MRPL12ENSG00000262814
SLC25A10ENSG00000183048
GCGRENSG00000215644
AC174470.1ENSG00000215621
FAM195BENSG00000225663
PPP1R27ENSG00000182676
P4HBENSG00000185624
ARHGDIAENSG00000141522
ANAPC11ENSG00000141552
ALYREFENSG00000183684
NPBENSG00000183979
PCYT2ENSG00000185813
SIRT7ENSG00000187531
MAFGENSG00000197063
PYCR1ENSG00000183010
AC137723.5ENSG00000235296
MYADML2ENSG00000185105
NOTUMENSG00000185269
ASPSCR1ENSG00000169696
STRA13ENSG00000169689
LRRC45ENSG00000169683
RAC3ENSG00000169750
DCXRENSG00000169738
RFNGENSG00000169733
GPS1ENSG00000169727
DUS1LENSG00000169718
FASNENSG00000169710
CCDC57ENSG00000176155
SLC16A3ENSG00000141526
AC132872.1ENSG00000184551
CSNK1DENSG00000141551
CD7ENSG00000173762
SECTM1ENSG00000141574
TEX19ENSG00000182459
UTS2RENSG00000181408
HEXDCENSG00000169660
C17orf101ENSG00000181396
C17orf62ENSG00000178927
NARFENSG00000141562
FOXK2ENSG00000141568
WDR45LENSG00000141580
RAB40BENSG00000141542
FN3KENSG00000167363
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs59606152chr1779952944hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr17:79953706-79953717GGAGGGTGTGG-6.32
MYCMA0147.3chr17:79953764-79953776GGGCACGTGGCC-7.22
PLAG1MA0163.1chr17:79953181-79953195GGGGCCCTGGGGGG+7.03
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_58054chr17:79953144-79953856VACO_9m
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177995279079952982
Number: 2             
IDChromosomeStartEnd
GH17I081993chr177995173479953753
GH17I081995chr177995384179953990
Enhancer Sequence
GGCCTGCTCT TGCTCACCCA GTCCCCGCTC ACTTTCAGCC CACTTTCCAA CTGGAAAATC 60
TGCTGTCCCG CAGCCGTCTC CAGGGCAGTG GCGGGAGACT CGGGCTCTTG AAAGCACGAC 120
GTGTTTCATG GAAAAAGAGG GAGTGGCCGG CCCTCGGAGC CCGGGCTGCC CCGAAACCTC 180
CCTCGGCGCC CTGTTTGTTT TTTCAGCTTC TCTCAAAGCC CAAGAGTCAC AAAAGTGGTT 240
TCATTTAATA AATATTTGCT TTGCTCGGTG TTTTGATCAT TTTCAAAACC GAGTGTGGCG 300
TGGCGCAAGC AAAGCCCGCC GTGGCGGGAC CCTCCTAGCG CTCGTCCCTG GCCTCACAGG 360
GGCCTTTTGT TTCCACGCTG GCTGAGTGCC CTTTGCTGGG GTGGGGGGGC ACTGGCCCGG 420
AGGGGCCCTG GGGGGCCAGG ACATTCCCCG CATTTATCCC CATTTGGAAG CTCCCTGGCT 480
GGGGCTGTGA CGGGGAGGTT CAGGTCTACG TCCTCCCTTG AGGGGATGAG CCACGGGGCT 540
CAGGACCCAG GCCCAGCACT GTCCTGAGGC TGTGGCCCTC AGGGACCCTT ACACCCTTTG 600
GCTTTTGTGC TGGGCCATTG ACTGTGCCCT CGCTAGAGGC AGCTTCTCCA CCCCTTCCTC 660
ACAGGTCAGA GTTAGCGTAT GGGACGTGGC CAGCCAGGCC CGATCCCTGC CCACCCCGAG 720
CTGAGCACCA GGAATGGCCA CCCCCGTGGG TGACAGCACG TTCCTGCCTC TCTCGCTCCG 780
GGCAGTGGGT CCTGGCACCA GGGCTTCCTC CTTGCAGCCC AGCTCTGCCA GCCCAGGCCT 840
CAGTGAGCTT GGGTCCCAGC TGCGGAGACC AGGCTGGGGG AGACACGGTC AGGCATGGGC 900
AGCAGGTCCT GCCCCGGCTG CAGACCAGAC TCAAGCTGGG CCTTGTGGAG GGTGTGGACC 960
GGCAGGGGCC AGATGTGGGG GGTGGGTAGG ATGGAGGCCA GAGAGGGCAC GTGGCCTGTG 1020
GTCCTGGTGG TGCCGGTGCC CGGAGGGCTT CCCTGGGCTC TGGGGTCCCG GTGCAAGGCG 1080
CACCTGTCCT GGCTGCTCCT 1100