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

TagContent
EnhancerAtlas ID
HS091-19772 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr17:40707230-40709090 
Target genes
Number: 55             
NameEnsembl ID
EIF1ENSG00000173812
ACLYENSG00000131473
CNPENSG00000173786
NKIRAS2ENSG00000168256
DNAJC7ENSG00000168259
KAT2AENSG00000108773
HSPB9ENSG00000197723
RAB5CENSG00000108774
KCNH4ENSG00000089558
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
AARSD1ENSG00000108825
RUNDC1ENSG00000198863
RPL27ENSG00000131469
IFI35ENSG00000068079
VAT1ENSG00000108828
NBR2ENSG00000198496
NBR1ENSG00000188554
TMEM106AENSG00000184988
ARL4DENSG00000175906
ETV4ENSG00000175832
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr17:40707869-40707880TTCTTATCTGT+6.14
Gata1MA0035.3chr17:40707869-40707880TTCTTATCTGT+6.62
PLAG1MA0163.1chr17:40708199-40708213GGGTCCCAGGGGGG+6.01
ZfxMA0146.2chr17:40707803-40707817CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_04349chr17:40705711-40708609Brain_Anterior_Caudate
SE_05405chr17:40705505-40709176Brain_Cingulate_Gyrus
SE_07457chr17:40705644-40708660Brain_Hippocampus_Middle_150
SE_08389chr17:40705452-40709281Brain_Inferior_Temporal_Lobe
SE_24066chr17:40705832-40707575Colon_Crypt_2
SE_25138chr17:40705027-40707582Colon_Crypt_3
SE_28881chr17:40705913-40707842Fetal_Intestine_Large
SE_29823chr17:40705821-40707851Fetal_Muscle
SE_57057chr17:40705585-40707606VACO_400
SE_57752chr17:40705855-40707551VACO_503
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr174070761940707836
chr174070799540708340
Number: 1             
IDChromosomeStartEnd
GH17I042556chr174070832140708470
Enhancer Sequence
CAGCACAGTG GCACCATTCC TTGAGCCCAG GAGTTGGAGG GTGCAGTGAG CATGATGGGG 60
CCACTGCACT CCAGCCTGGG TGACAGAGTG AGACCCTGTC AATTAATCAA ATGAACCAAC 120
CAACCGAAAA ACTCAGAAAC CAAGGTCCAG AAAGAAGCCA GCCCAGGATC ACACCTCAAG 180
TCCATATTAA AGGCCAGACA CAGTCTCTGG ATAACCAAGG GGCATCTGCA GGAGGAGTTA 240
GGTGGGAATT GGCTTGGGGT AGAGTCAGGT TGTGACTTGG ACCCCATTAG CCATGAGACC 300
TCAGGCAAGT TCCTTGCTTT CTCTCAGTCT TTCTTTTCTT TCTTTCTTTC TTTTTTTTTT 360
ATTTTCTGAG ACAGAGTTTC GCTCTTGTTG CCTAGGCTGG AGTGCAATGG GGCAATCTCG 420
GCTCACCACA ATCTCCGCTT CCCAGATTCA AGTGATTCTC CTGCCTCAGC CTCCCAAGTA 480
GCTGGGATAC CGGCTAATTT TGTATGTTCG GTAGAGACGG GGTTTCTCCA TGTTGGTCAG 540
GCTGGTCTCA AACTCTCGAC CTTAGGTGAT CCGCCCGCCT CGGCCTCTCA GATTGCTGGG 600
CATACAGGCA TGAGCCACCG CGACCGGCCC TCTGAGTCTT TCTTATCTGT AAAATGGGTA 660
TAATAATACC TATCTAATCG GTTTTAGTAA TGGTGGAGAT AATGCCTGAA AGTGCTAGTA 720
TAGAGGTTTA ATAGCCAGCA AGGACTGTTA TTAGAATGAA TAGTAATATG ACTACTGTCA 780
CATTTTGCAA ATGTGTAAAG AAGAAAGAGG GCTAAGTGAA TCAAAGGGAG ACAGCCCCAC 840
TCACCCTGTT CTGCCCCAGA GGACTGAGCG ATCCCCACCA TCTGGCAAGC TGCCTCACCA 900
GGAGGTCCAG CTGGGGCTAC AGGACTGGCT ACTTTGCTAC AATGGCCCGT CTTTCCTGAG 960
CCCAGTGGAG GGTCCCAGGG GGGCAGGAGT CATTGATAGG GGCCAGTAGG GTTGTAGAGC 1020
CACTGTCTGA ACTTCTGTGG AGGTCTGGTG CAGGGGAGGT GTGAACAGAT AGGAGGCTAG 1080
GTGAGGATGC AGCAGAGGAA GGGGGCAGGA GTGCCCCAGG AGGGGGCGGT ACCGAGGCAG 1140
GGATTCAGCT GGGTCTGAGA GGGAGGCAAG GCTGAGGGGG ATGGCCCTTT GGAGTGGGCA 1200
GGGACATGAC CACAGAAAGC CTGGGAAGTG GAAACAGACA GGAGCCTGTT GGAGCTCTTG 1260
GAGCTTTGTG TGGGGCACTG GGGGAAGGAG GCAGGCACTC CACCCTGACC TGCCCCTACC 1320
TCGGATGAGG GTCTTCTCTG CCTGTTGGAT GATGTGCTGC CCCTGCTCTT GGAGGAAGAG 1380
GCCTCCCAGC CACCCCCTCC TGCCAGTCGC CCTGACCTGC TGACCCAGAC AGATCTGCTA 1440
TCCCTACAGC ATCCAGGAAG GCCACAGGGA GGGGGCCCAG GTGGCATGGG TTTCTGAGGC 1500
CTGGGATCTG CTCTCAGTCC CGCTCTCGCC AACCCCCTTT GCCCCTCTGT GACAGTGTGT 1560
GTACATATGC GTGCATGTGT GTACCTGTGT GGTGTGGCTC ACAAGGTCAC CCCTGGGGGT 1620
GGGATAATAA GAGGTAAAGT GTGACCCCCT CTCTTCCGTA CATTCATTTT TTCAAGCTTG 1680
TGAATATTCA CATTGTTAAT ATAATCTTCT GCAGTCCCAT GACTTCGAAT AGCACTTAGA 1740
TGCCGATGAC CCCCCCACCA AAGAAACCCC ACTGTCTCCC ACAGACTCCA GGTCTGTATC 1800
TCCAACTGCC TACTCAATAC AACACGTCCA CCTGATGCAA TGAACTTAAT GTGTCTAAAC 1860