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

TagContent
EnhancerAtlas ID
HS129-00503 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr1:21650450-21652510 
Target genes
Number: 6             
NameEnsembl ID
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
TACAGGTATG CACCACCATG CCCGGCTAAT TTTTTTGTAT TTTTAGTAGA GATGGGTTTT 60
TGCCATGTTG GTCTGGCTGA CCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCAGCC 120
TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTTCACCC GGCCTGTTTT GTTTTTAAAG 180
AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC TTGACCATAG CCCATGCAGC 240
CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA GCGATCCTCT TGCCTCAGCC 300
TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC GGGCTCATAT AGCTTCTTAA 360
CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC AAGGGAGAAA CCATCCATCA 420
GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT GTGCTTCTGT CCAGGGAGAC 480
TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC TGACTGCCCT CTCCAGAGCT 540
GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA CAAGTTTGGA 600
GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC ACATGAAGAG AAACATTTCA 660
GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA GTCAGGCAGA 720
AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC AGAGATGGCT CTGGGCCCCA 780
GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA GCAGCTAGTG GAGTGTGCCA 840
GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC CAGCACTGCT CAAGTTGAAC 900
CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA GCTTTATGGC TGACTCACTG 960
CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA AGGAGAAAAA CAGTTCTCGT 1020
TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA GGAAAGCACA CATGTTTTGT 1080
TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA GGGGGGTTGA GACTGGTTGC 1140
AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC TTCATTAGCT GACACTAAAC 1200
ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG GCTCCAGGAC CACCAACCTG 1260
GTACCTGATG GCTTGTTTCT GCTCCCCACT CTTTCCCTCC ATGCATCTTT CTCTGAGCTT 1320
CTGCTCAAGG CAGGTGCCAG GACAAGCCAG CGTCTCGAGC GGTTCCCCTT CAGCGGTGAG 1380
AAGTAACGTC ACAATTAAGG GGCAAGAGGG GCCAGAGGAC AGAACAGTGC CAGTTCCTCA 1440
TCCAGATTGA AATTTGCTTC CAGCTGCCTG TCCCCACACC AGAAAGGGCA CTCCCTGCTC 1500
CCCATGCAGG CTTCTCATCC TCTTTTGCTG GCCTCCTCCC TCCTCGCTGT CCCTGGTCTT 1560
TTTCAGCCAC AAGCAAAACA CACTCAGCCT TGAAGTCAGA TGCTCTACAG AAGCCTGCAA 1620
AAACAGAGTC AGGAGTTGTG TGGCCTTGGC CGAGTCACCT CACCTCACCA AGCCTCAGCC 1680
TCCTCACCTA TTAAATGGGG ACACAATAGG ACCCACTTCC TTGGAGCTGA CTGAGGTATG 1740
AATTGAGTCA ATGCATTCAT TGCTCAGCAC ACAGCTTAGC TCAAAGTTAA TGCTCAATAA 1800
ATTGTGGTTC CCACCTCCTG CTCCACGGAG CAGACATGAA ACAGGTACGA GAAGCAACGA 1860
GAAGGGGCGG CAGCAGAGCA TCAACACACA GGGAGTCCTG CCTACTGTCC CGACGCCACC 1920
CAGAGGCTCA AGGGGTGCCC CGGCTGCTCT CCGAAGCTGC CGGTGGCACT TTCGCCAGCC 1980
ACCTTGTTTC CAAACTTGCT GCCAGCTTCC CCTAGCGCAG TGATTTCCAC AACGGAGCTC 2040
CCGGCTGTGG GAAGGGGGCT 2060