EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-15451 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr17:79392040-79395810 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7212578chr1779394536hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr17:79394296-79394311GGGTCAGACTGGCCT+6.24
EWSR1-FLI1MA0149.1chr17:79393229-79393247TCCTCCTTCCTGCCTCCC-6.08
EWSR1-FLI1MA0149.1chr17:79393233-79393251CCTTCCTGCCTCCCCTCC-7.49
Myod1MA0499.1chr17:79394198-79394211TGCAGCTGTTCCC+6.98
USF1MA0093.2chr17:79392128-79392139GCCACGTGACC+6.62
USF2MA0526.2chr17:79392126-79392142TGGCCACGTGACCTGT-7.25
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00395chr17:79390125-79398087Adipose_Nuclei
SE_01010chr17:79392619-79395878Adrenal_Gland
SE_01625chr17:79389351-79398706Aorta
SE_05872chr17:79388722-79398913Brain_Hippocampus_Middle
SE_26559chr17:79390386-79395974Esophagus
SE_28164chr17:79392457-79394609Fetal_Intestine
SE_29440chr17:79392485-79394550Fetal_Intestine_Large
SE_29667chr17:79391361-79395846Fetal_Muscle
SE_31439chr17:79390530-79395902Gastric
SE_34246chr17:79391602-79395908HCT-116
SE_40858chr17:79390369-79395795Left_Ventricle
SE_42181chr17:79390117-79398205Lung
SE_44415chr17:79390147-79395782NHDF-Ad
SE_47177chr17:79391538-79395537Panc1
SE_48277chr17:79391225-79395813Psoas_Muscle
SE_48718chr17:79390442-79395880Right_Atrium
SE_50245chr17:79389672-79395981Sigmoid_Colon
SE_51344chr17:79390313-79398121Skeletal_Muscle
SE_52635chr17:79390061-79395764Small_Intestine
SE_53447chr17:79391260-79395889Spleen
SE_54670chr17:79389831-79398114Stomach_Smooth_Muscle
SE_56968chr17:79392274-79394812VACO_400
SE_65328chr17:79390158-79401315Pancreatic_islets
SE_67997chr17:79358663-79398404TC32
SE_68398chr17:79359303-79407988TC71
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177939400079394317
Number: 1             
IDChromosomeStartEnd
GH17I081416chr177939054079398129
Enhancer Sequence
TGGAGAGGGC TTCAGATTGG AGAGGGTTCC AGGACAGCCC GAGAAACATT GGGTCCTGCT 60
TCTCCACCAC AGAGGGGAGC TGGGCCTGGC CACGTGACCT GTTGGCTGCC CGCCAGAATC 120
TACAAGACTC CCAAGGGCCA CTTTAGGGTC TGGGGTCTCA CTGCCCCAGG AGACGCAGCT 180
CAGAACTGAG CAGCTGTGCC GGGTCAGGGT CTGGTTCCCA TGCAGCAGTG GGCTGGGGGG 240
CTGGAGCTGC AACTTGATGG AGATCTGAGG CCCCCCTCTA CCACCAGTGG GCCGGGACAT 300
GCCCCGACCC AGGGCAGCTG TTCATCCCGG TGCCGCTTCA ATGCCACCTT TTGCACAGCG 360
GAGGCCAAGA GCCCTTGCCA AGGTTCAGGT CAGTAAGTGG ATAAGTCTGG TGGAGGCCTG 420
AGCCCTGGGA AGCAGCATCT TTGAGGACTT GCCCAGCTGT GTGGCTCCCA TGCCCGAGAA 480
CAGAGTCTGC CAAGGTGCGC ACACCCACAG ACGTGTGTGT GTGTACGTGT GTGTACGTGT 540
GTGTGTACGT GTGTGCGTGT GTGTGTGTAC GTGTGTGTGT GTGTGTGTGT GTAGCCACTC 600
ATCCCAGACA TGTAGCACAG TCAGACCTTG TGTGTACACC CATAGTCACG TGCATATGCC 660
CAGAGACAGG TTTGCACAGA CACACCCCGT GAGTCACACA CAGTCCCTCC CCTGCCTCTG 720
TGCAAGTGTG AGTGTGTGCA AGTGTGAGTG TGTGCAAGTG TGAGGTGCAC CCCACATCTC 780
GAGTCTGGAC CACTAGTGAT TGCAGCCAGG GTGGGGGAAG CATCACTGGG TTGTATCTGG 840
GGGTTGAGCC TGCAAACACC TGCACACCCA GCATGCACCT GCCTGTCTCC CAGCCACATC 900
TGCACACTGG GGTGGCATGT GGCTGGGCCT CTAGCCCCTG CCACAGCAGC TTCTGGTCTC 960
CTGGTGCGGG CGGAGGTCCC AGAGTGGCCT CTCACCCCAG GCAGAGCCTG GTCTCCCCAC 1020
CCCGTCCCTC ATTCCTCTTT CTGGGCAGCC AAATGGTCAG ATGCTACACC CCTGCCTCCA 1080
AGCAGGCTGC ACCTCCCCTC TGCATCCACG CAGGAACCTG TGCAGGGCGG CTTCCTCCCC 1140
GCGCTTTCCC GGAATGAGGA ATGTGGGGCA GGGCCAGCAG GGGGGCTGCT CCTCCTTCCT 1200
GCCTCCCCTC CCGTCCTGCA CAGCTCCCTT GGGAGCCTGG CTCGTGGGAA GTGTGCTTGG 1260
GACCGCCCAT CACTCCGTTC CCAGCCACTC CTGGTGTCCC CCGCCTGGGC GGGCCCTGTG 1320
GGGAGCGGGG AAGGTGTGGA GCGGAAGCCA GTGCCGAGGG AAGAGGGGAG CCTGAGTGGG 1380
TGTGGGTCGG GGGTGGGAGC TGACGCAGGC GGCGGGTGCA GCCGCCAGAC TCGGAGCCGG 1440
GGAGGCCCAT GCCAGCAGCC CGGCAGCTGG GCTTCCGGAA GCAGCGGGAG CCGGGAGCCT 1500
GGGAAGGGCC TCGCTGCTTC TCTGGAGCTG CCGCCATCTC AACGAGGCGT TTTTTTTTTT 1560
TTTTTTTTTT ACAACCCATT TCACAGTTTC CAGAAAAGGA GGATGCTGTC TCGGCGGCTC 1620
ACTTAACTCA AAACAAATGC TCGCTCTGCC GGCTCCGCGC CCGCCTCTCC CGGCTCCCGG 1680
GCCCTGCCGT CCTCTTGTTC CGTCTGCCTT CAGTCTGGTG CCACAGGGCG GAGCAGGGTC 1740
AGCCTGGCAG GAGAGTGGGG TGGGGCACAG TGGGCACCTG GCCATCCGAT TGCCCAGGCC 1800
CAGCCTCTGC TGTGTGGGTC CTCGGGACCC TGGATGGGGG CTGCTGGCAC GGCTGCTGGA 1860
CCGACCCTTA CAGAGGGAGT GGCTCTCCGG GGAGTCCTGG GCTCCAGGGC CCCAGCATGC 1920
TCTGTACCCC TCAGGCTGCC CAGCATGTGT TGCCCTTCTT AGCCATCCAT GGCAAGGAGC 1980
CTGGAAGACA GGTTGGCAGG AGGCAGGCTA GTTCCCATCG GCTGTCCTGG CCACTTAGGG 2040
CCACCTCTGC TGTAAGCCCA TGTGGCCAGC TCTCACCTAC TGTGTGCCGG CCTCCCCACA 2100
CAGCACCCCT GGGCCGGGGC CAGGCTCACT GGGCACCGAG ACTCCAGCCC AGCTGTTGTG 2160
CAGCTGTTCC CCAGTCTTCC CGCTGCTGGG CCACCCTGGG ACAGCAGGTC CAGGCACAGC 2220
CTGCCTCCTG GTCTAGTTGG CTGGACCTTG GGCTCCGGGT CAGACTGGCC TCCCAGGGAT 2280
GGGGCTGTGC CCGAGGACCT GAGCCACCTG GGGGTGGCCA CAGCCCTCCT GGTGTTGCTG 2340
TCTCCCGAAA CCATTTCCTC AGCTAGCCGG CCGCCCAAGC CAGGCCTCTA CAGCATCTTG 2400
GGCAGAGCTG AGGTGGCCCT GGAGCTGGGG CCAGAGCCCG GTCTGGATCT AGAGCTGCAA 2460
ACCCGGCCTG GGCCGGCTGG GCAGTGGGGG CAGCCAACTG GAGGCCAGTG TGCAGTCCTC 2520
GGTGGCCCCG CTGACACCGC ATCCCGCTTA CTGTCCCTTC CCCAGGAACA TCCTAAACTC 2580
ATGCTGCCTC CTGTGATGAG AGCTGATGGG AAGCCTGGCA GAGCGGCCCC AGGCAGGCTC 2640
TGTGTGGGGC CAGGGTGCCC TGACCATGCA CGCGGGTGGG GACAGGCCGT GTTCAGCCCC 2700
CAGCGGAGCA CTTGGGGCTA TGGGCCTGGA CCAGCAACTT AGACTTGGTC ATGCTCCATC 2760
TCTTACCAGC CCCATGGCGG GCCCACGACC GACCTTGGGA GCATGATGGC ACTACGTCAC 2820
ATGAGTCTGA AGCCCCAGGT AGGGGAGGTG CCACTGCAGG CAGTGCCAGG ATGGGGCACT 2880
TGGTCTGAGG AGGTCTAGGT CAAGACCCCC TCCCTGGCCC CCAGCTGCCT CCGCCTGGGC 2940
TGGTAACCAC AGCACTTCCT TTGCCAAGAG GAAAGAGCCC TCAGCCCGGT TCCCGGCTGG 3000
CCTTGGCCCA CACGGTCTGG CCCTGGCTGG AGCCCAGGCT ACACTCGGCT CCCAGGCAGC 3060
TGAGGCACAG GCTCTGTCTG GGGTTGGCCA CTGGTCGGCG GGGGGGCTGG GGAGGTGGCA 3120
GCCTGGTCTG CCCACGGCTC TGCTGGCCAG TCACGGTGCC ATCCCCAAAC ACCGGGAGGC 3180
GGGGGTGACA GTAGAGGCGT GATGCTCTGT CCTGGGGTTT CCCGGGCTCC TCGGGAGCTG 3240
AGTGGGATAG GGAGGGCCTC AGGTGGCCGG CAGTCCCGTC CCCCACACTC GCAGGGGTCA 3300
CCACAGTAGT GACCACCTGG CAGGGCCTGC AGAATCTGCT TCCAAGTTTC AAGCCAAGGC 3360
CAGGACAGTG GGGGAGAAAT CCACGCCTTT AGAGTAAGCA TCTGAGAGCC CCCAGCCGTG 3420
TGCAGGGCCC CTGCTCACGG GGCAAGGGGG ATGCCGGGCA GAGGCTCTTC CCCTGCCTGG 3480
TCCCGTCTCC GAGGTGCTGG CCTGCTGAGC AGCCAGTGAG ACGCCCTGGC AGCAGCTGCC 3540
GCCAGAGCCA GGATTTCCAG AAGCAAGAGG CCACCCCAGT CCCTTGGGGG GGATGGTAGG 3600
GTCTCTCATG GTAGGCTCAG TACGCAGGAT GCCTGGGCAC GGAATTGGGG TGCAGCATGC 3660
GACCCCATGT GATACTGGAG AAGGGTATTT GCAGCTGTGC CCAGAAGTGG TCCCAGAACG 3720
CTCATGCGAG GGCCTCAGGG CCGGGGTCTC GGGTGACTCC GCTTCCTCTC 3770