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

TagContent
EnhancerAtlas ID
HS147-00653 
Organism
Homo sapiens 
Tissue/cell
NHEK 
Coordinate
chr1:21650330-21652970 
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: 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: 3             
ChromosomeStartEnd
chr12165080621651685
chr12165078421652238
chr12165239921652754
Number: 1             
IDChromosomeStartEnd
GH01I021312chr12163897321657659
Enhancer Sequence
GACATAGTTT CACTCCATTG CCCAGGCTGG AGTGCAATGG TGCAATCTCG GCTCACTGCA 60
ACCTCCACCA CCCGGGTTTC AAGCTATTTT CCTGCCTCAG CCTCCTTGAG TAGCTGGGAT 120
TACAGGTATG CACCACCATG CCCGGCTAAT TTTTTTGTAT TTTTAGTAGA GATGGGTTTT 180
TGCCATGTTG GTCTGGCTGA CCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCAGCC 240
TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTTCACCC GGCCTGTTTT GTTTTTAAAG 300
AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC TTGACCATAG CCCATGCAGC 360
CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA GCGATCCTCT TGCCTCAGCC 420
TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC GGGCTCATAT AGCTTCTTAA 480
CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC AAGGGAGAAA CCATCCATCA 540
GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT GTGCTTCTGT CCAGGGAGAC 600
TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC TGACTGCCCT CTCCAGAGCT 660
GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA CAAGTTTGGA 720
GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC ACATGAAGAG AAACATTTCA 780
GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA GTCAGGCAGA 840
AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC AGAGATGGCT CTGGGCCCCA 900
GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA GCAGCTAGTG GAGTGTGCCA 960
GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC CAGCACTGCT CAAGTTGAAC 1020
CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA GCTTTATGGC TGACTCACTG 1080
CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA AGGAGAAAAA CAGTTCTCGT 1140
TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA GGAAAGCACA CATGTTTTGT 1200
TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA GGGGGGTTGA GACTGGTTGC 1260
AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC TTCATTAGCT GACACTAAAC 1320
ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG GCTCCAGGAC CACCAACCTG 1380
GTACCTGATG GCTTGTTTCT GCTCCCCACT CTTTCCCTCC ATGCATCTTT CTCTGAGCTT 1440
CTGCTCAAGG CAGGTGCCAG GACAAGCCAG CGTCTCGAGC GGTTCCCCTT CAGCGGTGAG 1500
AAGTAACGTC ACAATTAAGG GGCAAGAGGG GCCAGAGGAC AGAACAGTGC CAGTTCCTCA 1560
TCCAGATTGA AATTTGCTTC CAGCTGCCTG TCCCCACACC AGAAAGGGCA CTCCCTGCTC 1620
CCCATGCAGG CTTCTCATCC TCTTTTGCTG GCCTCCTCCC TCCTCGCTGT CCCTGGTCTT 1680
TTTCAGCCAC AAGCAAAACA CACTCAGCCT TGAAGTCAGA TGCTCTACAG AAGCCTGCAA 1740
AAACAGAGTC AGGAGTTGTG TGGCCTTGGC CGAGTCACCT CACCTCACCA AGCCTCAGCC 1800
TCCTCACCTA TTAAATGGGG ACACAATAGG ACCCACTTCC TTGGAGCTGA CTGAGGTATG 1860
AATTGAGTCA ATGCATTCAT TGCTCAGCAC ACAGCTTAGC TCAAAGTTAA TGCTCAATAA 1920
ATTGTGGTTC CCACCTCCTG CTCCACGGAG CAGACATGAA ACAGGTACGA GAAGCAACGA 1980
GAAGGGGCGG CAGCAGAGCA TCAACACACA GGGAGTCCTG CCTACTGTCC CGACGCCACC 2040
CAGAGGCTCA AGGGGTGCCC CGGCTGCTCT CCGAAGCTGC CGGTGGCACT TTCGCCAGCC 2100
ACCTTGTTTC CAAACTTGCT GCCAGCTTCC CCTAGCGCAG TGATTTCCAC AACGGAGCTC 2160
CCGGCTGTGG GAAGGGGGCT TTCTTTGACT TGTCCTAAAA TGGCCTCACC TGGACCCAGT 2220
GGGGTGTGGG GACCAGGGGG CTGGGCCTGG ACCTATGAGC ATGTTTCCTG CCTCCTCTCA 2280
GCCCCCATCC TTCTGCCGCC CCACGTTCTC AGCCAACAAT AGCTGCTTCC CAGACTCAGC 2340
TGCCACACAG CACGAGCTCC CTGAGCAAAA ATACCCATGC GGGGGAGGGT GGGGAGGTAC 2400
AGGAGGGGCC ACAAATGGGG AGGGCTGGGA GAAGGGGTGG CAGGATCAAG CTTGTCTCTT 2460
GAGTGCCTAC TGTGTGTCAA GCTGAGAAGG GTGAAGCCCC TGGGGGTTAG AGAAACCTGG 2520
GAGACCGTGG GGTGTGTGTG TCGGGGGTGC TGGTCTCTAA GACAGCAGAG CCTCCAGTCC 2580
CCAGAGAGGG ATCAGACCCA GGTCCAGGGT CTAAGGGTGA AGAAGGGGTC CAGGGAGAAG 2640