EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS091-19764 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:40689560-40690350 
Target genes
Number: 50             
NameEnsembl ID
ACLYENSG00000131473
CNPENSG00000173786
NKIRAS2ENSG00000168256
DNAJC7ENSG00000168259
DHX58ENSG00000108771
KAT2AENSG00000108773
RAB5CENSG00000108774
STAT5BENSG00000173757
STAT5AENSG00000126561
STAT3ENSG00000168610
PTRFENSG00000177469
ATP6V0A1ENSG00000033627
AC067852.1ENSG00000256929
NAGLUENSG00000108784
HSD17B1ENSG00000108786
COASYENSG00000068120
MLXENSG00000108788
PSMC3IPENSG00000131470
TUBG1ENSG00000131462
FAM134CENSG00000141699
TUBG2ENSG00000037042
PLEKHH3ENSG00000068137
CCR10ENSG00000184451
CNTNAP1ENSG00000108797
CTDENSG00000239671
EZH1ENSG00000108799
HMGN2P42ENSG00000214578
RAMP2ENSG00000131477
AC100793.1ENSG00000197291
VPS25ENSG00000131475
WNK4ENSG00000126562
CCDC56ENSG00000183978
CNTD1ENSG00000176563
BECN1ENSG00000126581
PSME3ENSG00000131467
AOC2ENSG00000131480
AOC3ENSG00000131471
RP11ENSG00000260105
AC100793.2ENSG00000213373
G6PCENSG00000131482
SNORA40ENSG00000212149
AARSD1ENSG00000108825
RUNDC1ENSG00000198863
RPL27ENSG00000131469
IFI35ENSG00000068079
VAT1ENSG00000108828
RND2ENSG00000108830
NBR1ENSG00000188554
AC087650.1ENSG00000237888
DHX8ENSG00000067596
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr17:40689576-40689597GTCCCTTCCCCACCCTCCTCT-6.16
ZfxMA0146.2chr17:40689755-40689769GAGGCCTAGGCGGG-6.24
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_01712chr17:40687048-40690755Aorta
SE_04349chr17:40688449-40689922Brain_Anterior_Caudate
SE_05405chr17:40686845-40690090Brain_Cingulate_Gyrus
SE_07457chr17:40686778-40689773Brain_Hippocampus_Middle_150
SE_08389chr17:40686872-40690621Brain_Inferior_Temporal_Lobe
SE_25138chr17:40687500-40689789Colon_Crypt_3
SE_29823chr17:40686923-40690027Fetal_Muscle
SE_35596chr17:40687190-40689876HepG2
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr174068994340690232
chr174068984840690200
chr174068960040689749
Enhancer Sequence
CGGGTGCGTG CCCACTGTCC CTTCCCCACC CTCCTCTATG GCGGGAGCCA CCGTAGGTGT 60
TTTCACCCGC CCCCCAGCAT GGGCGCAGTG TCTCTCTCTA GAAGTGCTTT CAGCGTGCAC 120
AGTGGCTTGG GCCTCCTAAA AACTGAGGCT TCCGGCCGGG CGCGGTGGCT CACGCCTGTC 180
ATCCCAGCAC TTCGGGAGGC CTAGGCGGGC GGATCAGGAG TTCAGGAGAT CGAGACCATC 240
CTGGCCAACA TTGTGAAACC CCGTCTCTAC TAAAATACAA AGAAATAGCA ACCTGGGCAA 300
CAGAGCGAGA CTCTGTCTAA AAAAAAAAAA AAAAAAAACT GAGGCTTCCA GTTTGAGGAG 360
TGGGGCTCCT TCCCCCATCT CCCCTATGCA GCCAATCACC TGGTCCCTTG GATCCAACTC 420
ATGGGCAGCT CTAGATCTGC CTCCCTGGAA GCTTCTGTGC TGCAATGGCT GCTCCAGGCT 480
CTGCTTAAGC TCTTCACACA GTTGCCCTGC CCTTCCATCT GGCACTCTTG CTCCATGAAG 540
CCTTCTAAGG CCTTCCTGTT GGGGGAAAGC CCCTTTGTGC CCCATCTCCT CACCCATGCG 600
ACAAAGGCAA CACAGTGAAC TCACCTACTC ACAGGTCTCT TTCCTCTGGG CTGTGGGCTC 660
CTTGATGGCA GCGTTCGGAT TTTGTCTCAG TAGCCCTAGC ACCCAGCACA AAGAAGCAAT 720
GAGTGAATGG TTGTTGAATG AATGAATGAA TGAATGAAGA TGAATATATT TCTATGTGTG 780
GGCCCTTCTT 790