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

TagContent
EnhancerAtlas ID
HS180-00712 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:21650500-21653540 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs213024chr121650664hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr1:21651121-21651135ATGACTCATTCTCC-6.04
JUN(var.2)MA0489.1chr1:21651116-21651130AAAAAATGACTCAT+7.52
Nkx2-5(var.2)MA0503.1chr1:21652787-21652798CTTGAGTGCCT-6.14
Number of super-enhancer constituents: 34             
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_03598chr1:21652795-21653500Brain_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_46660chr1:21653109-21654100Ovary
SE_47592chr1:21650567-21653016Pancreas
SE_47592chr1:21653087-21653622Pancreas
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: 3             
ChromosomeStartEnd
chr12165080621651685
chr12165078421652238
chr12165239921652754
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
GATGGGTTTT TGCCATGTTG GTCTGGCTGA CCTCAAACTC CTGACCTCAA GTGATCCACC 60
TGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTTCACCC GGCCTGTTTT 120
GTTTTTAAAG AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC TTGACCATAG 180
CCCATGCAGC CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA GCGATCCTCT 240
TGCCTCAGCC TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC GGGCTCATAT 300
AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC AAGGGAGAAA 360
CCATCCATCA GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT GTGCTTCTGT 420
CCAGGGAGAC TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC TGACTGCCCT 480
CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA 540
CAAGTTTGGA GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC ACATGAAGAG 600
AAACATTTCA GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA 660
GTCAGGCAGA AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC AGAGATGGCT 720
CTGGGCCCCA GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA GCAGCTAGTG 780
GAGTGTGCCA GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC CAGCACTGCT 840
CAAGTTGAAC CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA GCTTTATGGC 900
TGACTCACTG CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA AGGAGAAAAA 960
CAGTTCTCGT TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA GGAAAGCACA 1020
CATGTTTTGT TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA GGGGGGTTGA 1080
GACTGGTTGC AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC TTCATTAGCT 1140
GACACTAAAC ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG GCTCCAGGAC 1200
CACCAACCTG GTACCTGATG GCTTGTTTCT GCTCCCCACT CTTTCCCTCC ATGCATCTTT 1260
CTCTGAGCTT CTGCTCAAGG CAGGTGCCAG GACAAGCCAG CGTCTCGAGC GGTTCCCCTT 1320
CAGCGGTGAG AAGTAACGTC ACAATTAAGG GGCAAGAGGG GCCAGAGGAC AGAACAGTGC 1380
CAGTTCCTCA TCCAGATTGA AATTTGCTTC CAGCTGCCTG TCCCCACACC AGAAAGGGCA 1440
CTCCCTGCTC CCCATGCAGG CTTCTCATCC TCTTTTGCTG GCCTCCTCCC TCCTCGCTGT 1500
CCCTGGTCTT TTTCAGCCAC AAGCAAAACA CACTCAGCCT TGAAGTCAGA TGCTCTACAG 1560
AAGCCTGCAA AAACAGAGTC AGGAGTTGTG TGGCCTTGGC CGAGTCACCT CACCTCACCA 1620
AGCCTCAGCC TCCTCACCTA TTAAATGGGG ACACAATAGG ACCCACTTCC TTGGAGCTGA 1680
CTGAGGTATG AATTGAGTCA ATGCATTCAT TGCTCAGCAC ACAGCTTAGC TCAAAGTTAA 1740
TGCTCAATAA ATTGTGGTTC CCACCTCCTG CTCCACGGAG CAGACATGAA ACAGGTACGA 1800
GAAGCAACGA GAAGGGGCGG CAGCAGAGCA TCAACACACA GGGAGTCCTG CCTACTGTCC 1860
CGACGCCACC CAGAGGCTCA AGGGGTGCCC CGGCTGCTCT CCGAAGCTGC CGGTGGCACT 1920
TTCGCCAGCC ACCTTGTTTC CAAACTTGCT GCCAGCTTCC CCTAGCGCAG TGATTTCCAC 1980
AACGGAGCTC CCGGCTGTGG GAAGGGGGCT TTCTTTGACT TGTCCTAAAA TGGCCTCACC 2040
TGGACCCAGT GGGGTGTGGG GACCAGGGGG CTGGGCCTGG ACCTATGAGC ATGTTTCCTG 2100
CCTCCTCTCA GCCCCCATCC TTCTGCCGCC CCACGTTCTC AGCCAACAAT AGCTGCTTCC 2160
CAGACTCAGC TGCCACACAG CACGAGCTCC CTGAGCAAAA ATACCCATGC GGGGGAGGGT 2220
GGGGAGGTAC AGGAGGGGCC ACAAATGGGG AGGGCTGGGA GAAGGGGTGG CAGGATCAAG 2280
CTTGTCTCTT GAGTGCCTAC TGTGTGTCAA GCTGAGAAGG GTGAAGCCCC TGGGGGTTAG 2340
AGAAACCTGG GAGACCGTGG GGTGTGTGTG TCGGGGGTGC TGGTCTCTAA GACAGCAGAG 2400
CCTCCAGTCC CCAGAGAGGG ATCAGACCCA GGTCCAGGGT CTAAGGGTGA AGAAGGGGTC 2460
CAGGGAGAAG AAGGTGCCTA AGCAGGAAGC AGGTCCTAGA ACCTAGTGAG AAAAAAGGGG 2520
GGCCTGAACC CCAAAGAGAG ATCCAAATCT TAAGGAAAAT AGGGGCTCAG GTTCGAGGAG 2580
ATGAGGTTCA TAATAGGGGG GTTATATTTC TGGTTTCAGG AGGGGGATGG TTTGGAGCAG 2640
CGTAGGGAGG TGGGGCGAGG CCTGCAGAGC TAAGAATCCA TTTAACTGAG CAGCATCTCA 2700
GAGGTCTTAG GTGCCAACTG GGGTGACATC AGGGAAGAAA ACAGAAATCC TAAGACAGCA 2760
GCCAGCAGCC TGCAGTTACG GAGCCTGGAT GGGGAAGCAG CTCCCCGCTG CTGGGGAGAC 2820
CCCACTGAGC ACAGAGAGGG TCTCCCCAGC CTTTGGCCCC TGCGTCTCCT TTCTCTTCAT 2880
GACAGGGCAT CAGCTCGGGT CCCTGGAAAC ACCCCCGCTC CCCAGCAAGG GGCTGTGTTT 2940
GCACAGTGGC TCTGGCCCCT AAACCCCACC TCTGTGGACT CCGTCAAAGC CTGGGGAGGG 3000
CAGGGTCCTG AGGGCCCTGG TCTCGCTGGG GTCGCATAGG 3040