EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-00561 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr1:21650430-21652560 
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
CCTCCTTGAG TAGCTGGGAT TACAGGTATG CACCACCATG CCCGGCTAAT TTTTTTGTAT 60
TTTTAGTAGA GATGGGTTTT TGCCATGTTG GTCTGGCTGA CCTCAAACTC CTGACCTCAA 120
GTGATCCACC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTTCACCC 180
GGCCTGTTTT GTTTTTAAAG AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC 240
TTGACCATAG CCCATGCAGC CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA 300
GCGATCCTCT TGCCTCAGCC TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC 360
GGGCTCATAT AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC 420
AAGGGAGAAA CCATCCATCA GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT 480
GTGCTTCTGT CCAGGGAGAC TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC 540
TGACTGCCCT CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG 600
AGCTGAGGAA CAAGTTTGGA GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC 660
ACATGAAGAG AAACATTTCA GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA 720
GCTGAGCTGA GTCAGGCAGA AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC 780
AGAGATGGCT CTGGGCCCCA GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA 840
GCAGCTAGTG GAGTGTGCCA GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC 900
CAGCACTGCT CAAGTTGAAC CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA 960
GCTTTATGGC TGACTCACTG CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA 1020
AGGAGAAAAA CAGTTCTCGT TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA 1080
GGAAAGCACA CATGTTTTGT TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA 1140
GGGGGGTTGA GACTGGTTGC AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC 1200
TTCATTAGCT GACACTAAAC ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG 1260
GCTCCAGGAC CACCAACCTG GTACCTGATG GCTTGTTTCT GCTCCCCACT CTTTCCCTCC 1320
ATGCATCTTT CTCTGAGCTT CTGCTCAAGG CAGGTGCCAG GACAAGCCAG CGTCTCGAGC 1380
GGTTCCCCTT CAGCGGTGAG AAGTAACGTC ACAATTAAGG GGCAAGAGGG GCCAGAGGAC 1440
AGAACAGTGC CAGTTCCTCA TCCAGATTGA AATTTGCTTC CAGCTGCCTG TCCCCACACC 1500
AGAAAGGGCA CTCCCTGCTC CCCATGCAGG CTTCTCATCC TCTTTTGCTG GCCTCCTCCC 1560
TCCTCGCTGT CCCTGGTCTT TTTCAGCCAC AAGCAAAACA CACTCAGCCT TGAAGTCAGA 1620
TGCTCTACAG AAGCCTGCAA AAACAGAGTC AGGAGTTGTG TGGCCTTGGC CGAGTCACCT 1680
CACCTCACCA AGCCTCAGCC TCCTCACCTA TTAAATGGGG ACACAATAGG ACCCACTTCC 1740
TTGGAGCTGA CTGAGGTATG AATTGAGTCA ATGCATTCAT TGCTCAGCAC ACAGCTTAGC 1800
TCAAAGTTAA TGCTCAATAA ATTGTGGTTC CCACCTCCTG CTCCACGGAG CAGACATGAA 1860
ACAGGTACGA GAAGCAACGA GAAGGGGCGG CAGCAGAGCA TCAACACACA GGGAGTCCTG 1920
CCTACTGTCC CGACGCCACC CAGAGGCTCA AGGGGTGCCC CGGCTGCTCT CCGAAGCTGC 1980
CGGTGGCACT TTCGCCAGCC ACCTTGTTTC CAAACTTGCT GCCAGCTTCC CCTAGCGCAG 2040
TGATTTCCAC AACGGAGCTC CCGGCTGTGG GAAGGGGGCT TTCTTTGACT TGTCCTAAAA 2100
TGGCCTCACC TGGACCCAGT GGGGTGTGGG 2130