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

TagContent
EnhancerAtlas ID
HS091-19766 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:40693220-40695040 
Target genes
Number: 50             
NameEnsembl ID
ACLYENSG00000131473
CNPENSG00000173786
NKIRAS2ENSG00000168256
DNAJC7ENSG00000168259
DHX58ENSG00000108771
KAT2AENSG00000108773
HSPB9ENSG00000197723
RAB5CENSG00000108774
GHDCENSG00000167925
AC003104.1ENSG00000236194
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
RPL27ENSG00000131469
IFI35ENSG00000068079
VAT1ENSG00000108828
NBR1ENSG00000188554
TMEM106AENSG00000184988
ARL4DENSG00000175906
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs630539chr1740693344hg19
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_04349chr17:40694856-40695993Brain_Anterior_Caudate
SE_05405chr17:40694769-40696804Brain_Cingulate_Gyrus
SE_07457chr17:40694695-40696702Brain_Hippocampus_Middle_150
SE_08389chr17:40694767-40696034Brain_Inferior_Temporal_Lobe
SE_24066chr17:40692725-40693505Colon_Crypt_2
SE_24066chr17:40693510-40694022Colon_Crypt_2
SE_25138chr17:40692712-40694055Colon_Crypt_3
SE_28881chr17:40692606-40694128Fetal_Intestine_Large
SE_29823chr17:40694561-40696923Fetal_Muscle
SE_35596chr17:40692565-40694399HepG2
SE_57057chr17:40692969-40693927VACO_400
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr174069334640693790
chr174069406340694180
chr174069464340694756
chr174069480140694954
Number: 1             
IDChromosomeStartEnd
GH17I042540chr174069270240698177
Enhancer Sequence
GCAGGTACAG TGCCTGGGTG GGGTGGGAGA GCCCCCCAGA CCCTCAAAAA GAAGGGAGTA 60
GCAGATGTCA GTAGGGGTAG GCAGAGGGAC TGGAATAATG CCTCGCCATA ACACACAGTA 120
CTTCATAGTT TACCAAGCAC GTGTACACAT GCGTTGTCTC AGTGAATCCC ACTGTGGTTG 180
AGAGGTGAGC TCTGGAAGCC AACAACCTGG GTCACACCTC GCGCTCCTAT TTCCTGGCCG 240
TGTGACTTAT GACTCATGAC CTCCTTCCCA GTGTCTCGTT TGCTTTTCCT GTAAACTGGG 300
ACTACCTCAT AGGTAGAATA ACGCCTGGCC CAGAGCAAAG GCCACTAAGA GCTAGCTATG 360
AACAAGGATT TTGTTTCATC TCTGCGTGGT TGCTGAAGTA GGCACTGCAG GCAGGAGGTG 420
AGTGGATGTG CCTAAAGGCA CTAAGTGCGC ATCCTGCTAC AAAACTGTGA AGCCAGGGCT 480
CCTTCCTGCC ACTTAAAGGA GGAGTGGAGC AGAGGGCGCC CAAGTCAGGA ATGACTTAGT 540
GGAGAGGCGT CTGTGTTGGC CAGGAAGGGA ACAGATCAGC TCAGCCTTTC TTGAGCAGTA 600
CTGCTCCAAG TGTGACCCAA AACCAGCAGC AGCAGCAGCA GCAGCCCGAG CTGTGAGATG 660
GCAAATTCTC AGGCCCTACC CAAGACCTGA AGGAGAAGCT ACATTTTTTT TTTTTTTGAG 720
ACAGATTTCA CTCTGTTGCT GAGGCTGGAG CACAGTGGCA CAATCTCATC TCACTGCAAC 780
CTTCGTCTCC TAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTATA 840
GGCACCCGCC ACCACGCCCG GCAATTTTTG TTTGTTTTGA GATAGAGTCT CGCTCTGTCA 900
CCCAGGCTGG AGTGCAGTGG CACGATCTCA GTTCACTGCA ACCTCTGCTT CCTGAGTTCA 960
AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCGCCCC CCAACCACAC 1020
TCGGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCGC TATGTAGGTC AAGCTGGTTT 1080
CAAACTCCTG ACCTCAAATG ATTCGCCCAC TTCAGCCTCC CAAAGTGCTG GGATTACAGG 1140
TGTGAGCCAC CTTGCCTGGC CAATTTTTGT ATTTTTAGTA GAAACAGGTT TCACCATGGT 1200
GGCCAGACTG GTCTCAAACT CCTGACCTCA GGTGAACTGC CCACCTCAGC CTCCCAAAGT 1260
ACTGGTATTA CAGGCGTGAT CCACTGCGAC TGGCCTTGAT TTTGTTTTTG AGACAGAATC 1320
TTACTCTGTC GCCCAGACTG GAGTGCAGTG GCACAATCTC AGCTCACTGC AACTTCTGCC 1380
TCATGGGTTC AAGTGATTCT TGTGCCTCTA CCTCCCGAGT AGCCGGGATT ACAGGCACCT 1440
GCCATTACGC TAGGCTAATT TTTGTATTTT TAGTATAGAC AGGGTTTCCC CACATTGGCC 1500
AGGCTGGTCT GGAACTCCTG GGCTCAAGTG ATCCACCTGC TTCAGCCCCT CAGAGTACTG 1560
GGATTATAGG TGTGGGCCAC CACGCCCATT CAGAAACCTC CATGTTTTAA GGAGCCCTCT 1620
GGGTAACTCT CATGTTCACC CAAGCTGCTG AACCCTGTCC TGGAGTTTTC AGAGGGACGC 1680
GTATGTGCCA CAGAGCGTCC CGCTGGTGGG GGTCATGGGA AGCCATGACC TGGGATAGAC 1740
AGTCGTCTGT AGAGTGGGGT GAACATTCCC TGGGCCCTCT GTTTCATCAC TCCTCTTCTC 1800
TGTTCCCCCT ACCTCCTGTC 1820