EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS007-00210 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr1:21650380-21652130 
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: 1             
ChromosomeStartEnd
chr12165080621651685
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
GCTCACTGCA ACCTCCACCA CCCGGGTTTC AAGCTATTTT CCTGCCTCAG CCTCCTTGAG 60
TAGCTGGGAT TACAGGTATG CACCACCATG CCCGGCTAAT TTTTTTGTAT TTTTAGTAGA 120
GATGGGTTTT TGCCATGTTG GTCTGGCTGA CCTCAAACTC CTGACCTCAA GTGATCCACC 180
TGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTTCACCC GGCCTGTTTT 240
GTTTTTAAAG AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC TTGACCATAG 300
CCCATGCAGC CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA GCGATCCTCT 360
TGCCTCAGCC TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC GGGCTCATAT 420
AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC AAGGGAGAAA 480
CCATCCATCA GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT GTGCTTCTGT 540
CCAGGGAGAC TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC TGACTGCCCT 600
CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA 660
CAAGTTTGGA GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC ACATGAAGAG 720
AAACATTTCA GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA 780
GTCAGGCAGA AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC AGAGATGGCT 840
CTGGGCCCCA GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA GCAGCTAGTG 900
GAGTGTGCCA GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC CAGCACTGCT 960
CAAGTTGAAC CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA GCTTTATGGC 1020
TGACTCACTG CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA AGGAGAAAAA 1080
CAGTTCTCGT TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA GGAAAGCACA 1140
CATGTTTTGT TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA GGGGGGTTGA 1200
GACTGGTTGC AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC TTCATTAGCT 1260
GACACTAAAC ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG GCTCCAGGAC 1320
CACCAACCTG GTACCTGATG GCTTGTTTCT GCTCCCCACT CTTTCCCTCC ATGCATCTTT 1380
CTCTGAGCTT CTGCTCAAGG CAGGTGCCAG GACAAGCCAG CGTCTCGAGC GGTTCCCCTT 1440
CAGCGGTGAG AAGTAACGTC ACAATTAAGG GGCAAGAGGG GCCAGAGGAC AGAACAGTGC 1500
CAGTTCCTCA TCCAGATTGA AATTTGCTTC CAGCTGCCTG TCCCCACACC AGAAAGGGCA 1560
CTCCCTGCTC CCCATGCAGG CTTCTCATCC TCTTTTGCTG GCCTCCTCCC TCCTCGCTGT 1620
CCCTGGTCTT TTTCAGCCAC AAGCAAAACA CACTCAGCCT TGAAGTCAGA TGCTCTACAG 1680
AAGCCTGCAA AAACAGAGTC AGGAGTTGTG TGGCCTTGGC CGAGTCACCT CACCTCACCA 1740
AGCCTCAGCC 1750