EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-00817 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr1:21650400-21652650 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs213024chr121650664hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr1:21651121-21651135ATGACTCATTCTCC-6.04
JUN(var.2)MA0489.1chr1:21651116-21651130AAAAAATGACTCAT+7.52
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00105chr1:21640019-21654616Adipose_Nuclei
SE_00854chr1:21648312-21655068Adrenal_Gland
SE_01643chr1:21650385-21655084Aorta
SE_02944chr1:21650503-21654392Bladder
SE_03598chr1:21650640-21651193Brain_Angular_Gyrus
SE_03598chr1:21651214-21652589Brain_Angular_Gyrus
SE_04518chr1:21650430-21654343Brain_Anterior_Caudate
SE_05710chr1:21650819-21652666Brain_Cingulate_Gyrus
SE_05944chr1:21650172-21654641Brain_Hippocampus_Middle
SE_08398chr1:21650274-21654628Brain_Inferior_Temporal_Lobe
SE_08982chr1:21651888-21652526Brain_Mid_Frontal_Lobe
SE_26127chr1:21650420-21654272Duodenum_Smooth_Muscle
SE_26770chr1:21650381-21654470Esophagus
SE_28486chr1:21650385-21652524Fetal_Intestine
SE_29337chr1:21650482-21652798Fetal_Intestine_Large
SE_31433chr1:21650314-21655007Gastric
SE_39164chr1:21650503-21653287IMR90
SE_42174chr1:21650278-21654424Lung
SE_44380chr1:21650380-21654322NHDF-Ad
SE_45045chr1:21650463-21654349NHLF
SE_46660chr1:21650609-21653070Ovary
SE_47592chr1:21650567-21653016Pancreas
SE_48583chr1:21650390-21654421Right_Atrium
SE_50108chr1:21650386-21654252Sigmoid_Colon
SE_52633chr1:21650385-21654180Small_Intestine
SE_53334chr1:21650242-21653182Spleen
SE_54639chr1:21650371-21654862Stomach_Smooth_Muscle
SE_56171chr1:21650384-21653718u87
SE_65263chr1:21650278-21654762Pancreatic_islets
SE_67931chr1:21650384-21653718u87
SE_68932chr1:21650478-21654339H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12165080621651685
chr12165078421652238
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
CCCGGGTTTC AAGCTATTTT CCTGCCTCAG CCTCCTTGAG TAGCTGGGAT TACAGGTATG 60
CACCACCATG CCCGGCTAAT TTTTTTGTAT TTTTAGTAGA GATGGGTTTT TGCCATGTTG 120
GTCTGGCTGA CCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCAGCC TCCCAAAGTG 180
CTGGGATTAC AGGCATGAGC CACTTCACCC GGCCTGTTTT GTTTTTAAAG AGACAAGGTC 240
TCACTCTGTT GCCCAAGCTG GAGTGCGGCC TTGACCATAG CCCATGCAGC CTCGACCATA 300
GCTCATGCAG CCTTGACCTC CTGGGCTCAA GCGATCCTCT TGCCTCAGCC TCCCAAGTAG 360
CTGGGACTAC AGATGTGCAC CACCACACCC GGGCTCATAT AGCTTCTTAA CTGGGTGGGC 420
AGAGGAAGCA GGGGGCAGAG GCCCATCCCC AAGGGAGAAA CCATCCATCA GTGCGGGACT 480
GACAGGGACA CTCCACCCAC TCAGCCCAGT GTGCTTCTGT CCAGGGAGAC TCCAACGGCT 540
GCCACAGCTG TGGTTTACTG ACTTCAGGTC TGACTGCCCT CTCCAGAGCT GCCCTAGAAT 600
CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA CAAGTTTGGA GAGGACCAGG 660
AGGGGCTCTC CCCACCCCCG CCCCTTTCCC ACATGAAGAG AAACATTTCA GGGTTGAAAA 720
AATGACTCAT TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA GTCAGGCAGA AGGAGCCCGC 780
GGGTCACTTA ATCGGCCTCC CTGCTCTGGC AGAGATGGCT CTGGGCCCCA GGAAGCCAGG 840
GACAAATGGA GGCGGAGGTG GCAGAGATAA GCAGCTAGTG GAGTGTGCCA GCCTCTCCTT 900
CCCCAACCGA GTGTGTCACT GGGCGTCACC CAGCACTGCT CAAGTTGAAC CTGATGCAGA 960
AGAAAAATTC CTCTGGACTT TCCTGAACGA GCTTTATGGC TGACTCACTG CCACCTGGAG 1020
CCTGCAAGAA AAGTCACAAA TCACGAAAGA AGGAGAAAAA CAGTTCTCGT TAAGCCATGT 1080
CTTCAATGGA GGTATCAGAG GTCGCCAGGA GGAAAGCACA CATGTTTTGT TGTGGGTTTC 1140
CTTCTCTAAA GAAACACGTT ACACAATAGA GGGGGGTTGA GACTGGTTGC AAAACTGCAA 1200
AATCCAATTT TGTGTACTGG ATTCAATTTC TTCATTAGCT GACACTAAAC ACAGAGACGG 1260
GGCCCTTGTG ACTAGATGAA CCATAAACTG GCTCCAGGAC CACCAACCTG GTACCTGATG 1320
GCTTGTTTCT GCTCCCCACT CTTTCCCTCC ATGCATCTTT CTCTGAGCTT CTGCTCAAGG 1380
CAGGTGCCAG GACAAGCCAG CGTCTCGAGC GGTTCCCCTT CAGCGGTGAG AAGTAACGTC 1440
ACAATTAAGG GGCAAGAGGG GCCAGAGGAC AGAACAGTGC CAGTTCCTCA TCCAGATTGA 1500
AATTTGCTTC CAGCTGCCTG TCCCCACACC AGAAAGGGCA CTCCCTGCTC CCCATGCAGG 1560
CTTCTCATCC TCTTTTGCTG GCCTCCTCCC TCCTCGCTGT CCCTGGTCTT TTTCAGCCAC 1620
AAGCAAAACA CACTCAGCCT TGAAGTCAGA TGCTCTACAG AAGCCTGCAA AAACAGAGTC 1680
AGGAGTTGTG TGGCCTTGGC CGAGTCACCT CACCTCACCA AGCCTCAGCC TCCTCACCTA 1740
TTAAATGGGG ACACAATAGG ACCCACTTCC TTGGAGCTGA CTGAGGTATG AATTGAGTCA 1800
ATGCATTCAT TGCTCAGCAC ACAGCTTAGC TCAAAGTTAA TGCTCAATAA ATTGTGGTTC 1860
CCACCTCCTG CTCCACGGAG CAGACATGAA ACAGGTACGA GAAGCAACGA GAAGGGGCGG 1920
CAGCAGAGCA TCAACACACA GGGAGTCCTG CCTACTGTCC CGACGCCACC CAGAGGCTCA 1980
AGGGGTGCCC CGGCTGCTCT CCGAAGCTGC CGGTGGCACT TTCGCCAGCC ACCTTGTTTC 2040
CAAACTTGCT GCCAGCTTCC CCTAGCGCAG TGATTTCCAC AACGGAGCTC CCGGCTGTGG 2100
GAAGGGGGCT TTCTTTGACT TGTCCTAAAA TGGCCTCACC TGGACCCAGT GGGGTGTGGG 2160
GACCAGGGGG CTGGGCCTGG ACCTATGAGC ATGTTTCCTG CCTCCTCTCA GCCCCCATCC 2220
TTCTGCCGCC CCACGTTCTC AGCCAACAAT 2250