EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-10278 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr13:114829600-114832680 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr13:114831180-114831195GGGTCACACAGCCCT+6.01
IRF1MA0050.2chr13:114830067-114830088AAAAGAAAAATGAAACCGGCT-6.27
MLXMA0663.1chr13:114830742-114830752ATCACGTGAT+6.02
MLXMA0663.1chr13:114830742-114830752ATCACGTGAT-6.02
MLXIPLMA0664.1chr13:114830742-114830752ATCACGTGAT+6.02
MLXIPLMA0664.1chr13:114830742-114830752ATCACGTGAT-6.02
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_00138chr13:114827062-114835371Adipose_Nuclei
SE_00817chr13:114830145-114830505Adipose_Tissue
SE_03425chr13:114828941-114831797Brain_Angular_Gyrus
SE_04238chr13:114828827-114832657Brain_Anterior_Caudate
SE_05108chr13:114827606-114834983Brain_Cingulate_Gyrus
SE_05953chr13:114828885-114835100Brain_Hippocampus_Middle
SE_07043chr13:114828880-114835230Brain_Hippocampus_Middle_150
SE_08101chr13:114828923-114832389Brain_Inferior_Temporal_Lobe
SE_09714chr13:114827574-114835404CD14
SE_17352chr13:114828918-114835297CD4p_CD25-_CD45RAp_Naive
SE_18337chr13:114828780-114835034CD4p_CD25-_Il17-_PMAstim_Th
SE_22425chr13:114829000-114835146CD8_primiary
SE_30552chr13:114828907-114835038Fetal_Muscle
SE_34578chr13:114828908-114832944HCT-116
SE_39266chr13:114828826-114835076IMR90
SE_43356chr13:114828948-114835116Lung
SE_43778chr13:114828945-114835312MM1S
SE_44448chr13:114827784-114835135NHDF-Ad
SE_44958chr13:114828684-114835047NHLF
SE_46283chr13:114827829-114835063Osteoblasts
SE_50768chr13:114828922-114835063Sigmoid_Colon
SE_53836chr13:114828807-114835313Spleen
SE_58808chr13:114808446-114835298Ly1
SE_67256chr13:114828945-114835312MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr13114831603114832299
chr13114831090114832324
Number: 1             
IDChromosomeStartEnd
GH13I114062chr13114827994114835274
Enhancer Sequence
GTCACCAGTG GGTGACTATG GACCTGTGAT CAGCCAACTC TGAAATGAGC TCCAGCAGAT 60
GGACACAGCG TCCCAGGACC TGCAGGAGCA GAGGCTGCGA GGCCAGCCAC GTCCACCTCG 120
ATCACGTCAC CTCGTGGGCA GAATGGCCTA CGCCCCATGT CCTCCCAGCC CCACCCAGAA 180
CCCACGGTGA GCACCCGGCA GGAAGTGGCC ACAGCACCAT CACTGGAGGC CACGCGGAGT 240
CTGAGGACAG CAGCTTTCCC CCCTATGCTG TTGTGGGGAC TCCAGGCTCA GCCTGAGGAC 300
AGGGTCAGTT CCCTCCACAC AGCACCAACA CTCCCAGGTG CAAAGCCCAG GCCCACGGAC 360
AGCCCCCCGC TGTCCGTGGG TCTCATGGTG GGGGCACCCA TTTTCTTTCA TCAGCAGGAA 420
GGTTTGTGCT TTCTCCTTCC TGGGCAGCAG AGTTTGAAGC GTATTCCAAA AGAAAAATGA 480
AACCGGCTGA ACGCTAGGGC ATTCCTCCCA TCCCCCATCC TGTTCGGTGG CCTGTGCCGG 540
ACAATCTCTT CTTTCTGATG GACTCAAAGG GGCCACACAG CCACCAGGTG CCCCCCTTCC 600
CATCAGCAGC TTAACCTCGG GGTATCTCTT GGACAGGCCG GCTTTGTCTC CAGCCGAGGT 660
CAGCAGCAGT CAGATGCGGG ATGAATGCCT GGCCCAGGCG GCCCCCACTC ACCGCCCGAG 720
GGCTCTGGAA CTCTCTTTCC AAATAAAGAA AAAGTGCGGC CTGAGAGGAC CAGGCTCGCC 780
TGAAATCCTG CCATGTGGCC TAAGGAAATT AACGCACGCA GCAGCCTCTC CCTCTGAGGC 840
AGAGACCCTG GCAAAGTCTC CTTTCCCTCA GTCATTTCTG GAAGAAGTGC AAATGAAGTT 900
TCACAGAATC AAGCAAACTT TCACGGGGAA AAAAGAAAAA ACCTCTTGCA GAAAACAGAG 960
TTGACCTTTA AGTAGTGGCT CTGATGAGGG GAAACCATCT GAACTGAATT CCTCCTCCTC 1020
CTGGAGCCTG GAGCAGGGGC TCAGCTGGGA CCAGCAGAGA AACCCCCGCC TTCTCCTCCC 1080
TGAGTCACTT CCCAGCATCT GCGCAAGGCT GGCGCTGCCC CATCCCGCCT GCGGCTGCTC 1140
CCATCACGTG ATCATAAGAA AATAAACCTG GTTTCCCAGC TCTGTGCTCT GCCGCAGGCT 1200
CGGGGCCCAT TTCCCAAACG CTGGGGGGAG CCGGGAGCTG CCAGGGCTGC CCCAGCCTCG 1260
GGGTAGAGGG TAAAGGCTGC GTGAAGAGGA ACCAAACCCC AAACCGGGTC TGCGAAGCAG 1320
CCCTGGGGCT CCCAAGCCAG CCTCTGGGCT GAGCTCTGCG GTCCTGAGTC ACTGCCTGAC 1380
TCATCCTCAG AGGCGCCCCA CAGAGAAGGG GCAACTTGGC CAGGGAAAAT GCTCCATCTC 1440
CGCAAAGGAC AGGAGGCAAA ACACACCCAT CAGAAGCACA TGGCCAGTGC AGGGCCACAC 1500
AGCCCTGGCT CCCACAGACC GCAGGCTGGA GAATGGGGGT CCGCGGTCAG CTCATAGCCC 1560
ACCCGCCACC CAGCACTGCA GGGTCACACA GCCCTGGCTC CCAGAGGTCA GAGGCTGGAG 1620
GGCAGGGGTC CGTGGTCAGC TCACAGCCCA CTCACCACCC AGCACGGCAG GTCTCAGCGG 1680
AAGCCCCACA CACACTGGGT TGCAGCCTCC TGTGGTTCAA GATGGGTGGG GTTATTTTGA 1740
AATGTTGGCA AATAGAGCTG TGAGTCTTCA AACGGAACCC AAAGACTCAG TGAGGAAAGC 1800
AGGCGGGCTG GGCTGAGACT CACAGCTGCA GCGGCCGTGG TGAGCCACCT CACCTCCCCG 1860
AGCCTCAGTC TCCCCATCTG TTCAGGGGCA CCGAGGAGCT GCCCCTCGGC TCATGGGCTC 1920
TGTGGTCGCC AGGCACGCCA CACACCACAC GCCACACACC ACTGCACGCA GCACCCCGGG 1980
ACACTGTGGC CTCGGCTCCC GCCTCTCCTG CACATGAGGC TCTTTCCTCT CTCCCACCCC 2040
ATACCCCCCA AAAAAGAACC ACCATCCTTA CAAACAAATG AAAATCGGCT GGGTCTTTAG 2100
GGCCCGGCCA CGATGTGTGA CTGCAGCAGT GACTCTCAGG AGGAGGCACA ACCAGACACC 2160
GGGTCCCCTG CAGCAGCTGA GACACCTCAA ACCCCAAACC CTCAGTGAGG CCCTGGTGGG 2220
AAAAGGGGCT CTCCAGGGAG GTGCCAGGGG CAGGAGAGAG GGCCAGCGGC CGAGGAGCGG 2280
GAGGCGGCCG GGCGAGAGGA GGCCCGGGCA GGAGGGAGAA GGGGGGACCT GGCCTTTGCT 2340
CCTCATGGGA TCCTCGGTGC GGCCCCCTCG TGACAGGCCC AGCCTCTCCC TGCAGTGGCC 2400
CAGCCACAGC TCAGGGCCAG GAGGCTCCTG CAGGCACAGG CGGCCGATGA GTCCCTTCCA 2460
GGCCTGGGCC TGGGGCAGCC TGCCATGTGC AGTAGACACT CAGTACTCAC AGAATACGAG 2520
CAACCTCATG CTCTCCGCCG GCTGAGTTCC TGTGCGGCTG AGAGAACCCC CTGCATCATT 2580
CTGACACAGG TGCGCTCCTG TGAGCCAGCA TGACACGGAA GGACACACAC ATGCAGGTGG 2640
AGATGGAGAT GCTGGGCCGG GCTTGGGGGT CATACAGACA GGACCAGGGG CTCTGACCTG 2700
CTGGGAGATT TGGGGCCAGC ATTCCAGGAC TGAGAGAACA GATCCCTGGC CTGGGGTGCT 2760
CTGGGGCTGA GGATGGGCCC CCACCTGGGC TGAGGATGGG CCCAACCTGG GCTGAGGACG 2820
GGCCTCCCCA CCTGGGCTGA GGACAGGCCC CCCTACCTGG GCTGAGGACG GGCCCCCCAA 2880
CCTGGGCTGA GGACGGGCCC CCTGACCTGG GCTGAGGACT GGCCCCCTGA CCTGGGCTGA 2940
GGACAGGCCC CCCAACCTGG GCTGAGGATG GGCCCCCCAG CTGGGGCACT CTGGGGCTGA 3000
GGACGGGCCC CCCACCTGGG GCACTCTGGA GCTGAGGATG GGCCCCCACC TGCGGTACTC 3060
TGGGGCTGAG GACGGGCCCC 3080