EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-22689 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr22:43333060-43337190 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEOX1MA0661.1chr22:43335850-43335860GCTAATTAAC+6.02
ZNF263MA0528.1chr22:43336460-43336481TCCTCCTCAATCCACTCCTCC-6.24
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_01645chr22:43332134-43336934Aorta
SE_09286chr22:43324019-43335350CD14
SE_09286chr22:43335391-43336474CD14
SE_10803chr22:43332662-43334162CD19_Primary
SE_11154chr22:43323646-43337116CD20
SE_25902chr22:43324116-43337807Duodenum_Smooth_Muscle
SE_27204chr22:43332782-43336988Esophagus
SE_30234chr22:43334728-43336890Fetal_Muscle
SE_31403chr22:43332769-43334140Gastric
SE_31403chr22:43334181-43337030Gastric
SE_36815chr22:43332805-43337225HMEC
SE_37119chr22:43332583-43337260HSMMtube
SE_38670chr22:43332931-43337592HUVEC
SE_40836chr22:43332829-43337196Left_Ventricle
SE_41751chr22:43334373-43334891LNCaP
SE_41751chr22:43334951-43335369LNCaP
SE_41751chr22:43335397-43336754LNCaP
SE_42274chr22:43332771-43337082Lung
SE_44283chr22:43332766-43337897NHDF-Ad
SE_45407chr22:43332915-43334185NHLF
SE_45407chr22:43335077-43336961NHLF
SE_45700chr22:43332169-43337245Osteoblasts
SE_47465chr22:43332998-43334063Pancreas
SE_47465chr22:43334171-43336305Pancreas
SE_47465chr22:43336437-43336922Pancreas
SE_48675chr22:43332973-43336811Right_Atrium
SE_50912chr22:43332840-43337147Sigmoid_Colon
SE_51895chr22:43333041-43334123Skeletal_Muscle_Myoblast
SE_51895chr22:43335432-43336901Skeletal_Muscle_Myoblast
SE_53064chr22:43332775-43337427Small_Intestine
SE_63694chr22:43332994-43334123HSMM
SE_63694chr22:43335283-43336915HSMM
SE_65321chr22:43332744-43336002Pancreatic_islets
SE_65321chr22:43336046-43337275Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 8             
ChromosomeStartEnd
chr224333311443333962
chr224333434243334403
chr224333443843334859
chr224333605443336708
chr224333672543336853
chr224333351143333722
chr224333432343337160
chr224333320043334221
Number: 1             
IDChromosomeStartEnd
GH22I042928chr224332486943337440
Enhancer Sequence
GTGTTCTGAA TGCTGGGAAT CTAACAGCGG AGAGAACAGA CCAAAACTCC TGCCCTCATG 60
GGTCTGTGTT CTGGCACAGG TGACTGACCC AGCAGGTGCT ATGCAGAGAA ATAAGCGAGG 120
ATGAGATAGG GAGGAGACAG AAAGGAGACT GCTTCTAAAC AGAGTGACCA GAGAAGGTCC 180
CCAAAGAAGG TGACACCTGA GACAACATGG GAAGAAGTAA GCCATATGGG CCCCCAGAGC 240
ACAGGCAGCC CCAGCAAAAG GCAAGAGAGG CCCACCTGGC ATGTCTGAGG CACAGAAAGA 300
CAGGTGTGGC AGCAGTTCCT GGTGAGATGG CTGTGGGTGA GCCCAGGCAG GCGGCAGTAG 360
AAATAACGAT GCATGAGCTT AAACGGGCAC CGAAGACAAA ACAAAATGAC CTCTTTGTTC 420
AACTTCTAGC CCCACCACCA AAGTCCACCT CTGAGCCCCT GCCTAGATGT CCCGGCTCGA 480
TCACCAAGGT TGTGTGCAGT GACTACCACA CACTGAATCT CCACACGGCC TCATTCTCAA 540
GGAGCCCTGT GCAAGCAGTC AGGCATGTGA GTCAGCATAC GAGGTGCTTT CACTTACCAC 600
ACCCCTTGCC TGGCCACAAA TCCTGCACTT CCCCTAACTC GGCTCTCCCT CAGACTCAAC 660
CAAGGCCCCA CTGTGGGTGA GGAGCAGGGA CACTGGCTCC CAGCCCTTTC CATGGCACCC 720
ATGCAGCTCC GAGAACAGCA AAGTCCAGCA TCCCTAGGGG GTCACACGAT CTGAAGACCA 780
GTCACACAGA CATGGAGCCC CGCAGGGGGA CCCTTCTCCT GGCTCGAGCA GTCTGGACCC 840
CCATCTCCAG AAGGCTTCAA TCTCCCACTG GAGAACTCTG GAATGACAGC GGTAGAAGTC 900
TCACCTGCGC CTGCCTGGTT GATTTTTCCC AGCTAACTTG CTCCCTGCCC TCTACCCACA 960
GTTGTACAGA GTAAAACAAA ATCATCATGT TAAATACTAG ATTCTAGATG ACAGCCCTAA 1020
AAACGACTGC CATTTAAGTC GAGCAAAATT TAAAATCTTT TTGAAACAAA CCAAGCAATC 1080
ACTTGAGGTA AGTTTGGGGA AGGTCTTTTG AAATCAATCA CTCTCTCCAC TGGAGATCCA 1140
GTTTCCAAGT TGTTTCCTGG GCTCGCGAAG CAGCAGAAGG TATGAATAGA GAATGCTAGG 1200
CAGTGAATTC CTAAAACCCG AGGATGAAAA CACACACGGT TCTGAAGATC CCACAGAAAG 1260
ATATGCCAAT TAATCTTATT CTTAAAATTG GCCTGAAGAA GAAAGGGAAG CCCCTGATGC 1320
AGAAACTGCA TAAGGAATCC TCCCCTCTGG AACACACAGG AGGCGTCAGA AAGAAGCCTG 1380
ACCTTCTCCC TTTCCCATGA CCTTAGAGGA AAGGAAGGTC AGTCACAGCA GCAGTGGCTC 1440
AGAAGCAGGT AGGGAATCTT TTTCTATGGG AAGAGCTCAC CAGGTGTGTG CTGTGTGCCA 1500
AGGACCACAG CAAGCAGAGG CTGTCCAAAC ATGAAGAATG CCTCTGCACA GGCCAACTGC 1560
ATGTTCCGCA GGACCATTTA GGTTGCACCA TCTCCCTCTC GACAGCCTGG CACAGTGGCA 1620
TTCCGGTGTG TGCTACCCGT GCCTGGCTGG TGAAGAGCCT TTCTCCCACT CCACCTGGAG 1680
CTCCACGAGG GAAGGGCTTC ACCCTTTTTA TCTAACCCAA AGCAAGTGCT CAAGTAACAA 1740
GAGAAGACGA CAAGGGAAGG GAAGAGAGGA GGTGCTGTTT GTGCTGGATC CCGAGGTGGA 1800
GAAGGTAAAA ATGCTGTCTG TGACAAATTT GTATTTTTTA AAAATCCTAT ATGCAGATTC 1860
ATATAGTAAC CCTTAAAATA ACCATGTTTT CCCCAACATC TTTATAGGTC AAAGGAAACA 1920
AGCTGATGAC CAGCCATCCT GGTGGCATTC AGACCGCTTG CTCCAGCTGA CAACCACCTG 1980
GGCTATCAGA ATCAGCAGCA AAGGTAGGAC AGGCCCCAAG GTCACCCGTC CCAGCGCAGC 2040
CCATCAGCTC TTAGCTCACC TATGCAACTT AATGAAGAGC TGGAGCTAAC AGCGTGTAAT 2100
TAGATGTGTC CCCAAAACTC GTTTATCTTA TGCAATGGGA ACACATCAGC TGACAGATCC 2160
AGACTTGCCT TGGACTGATT TTTACAGCAA TATTTTTTTA GCCTCTGGTT GGCAAGCACC 2220
CTGGGAATGT GGAGATGGAG GCTGAACACT TCCCCAACCT AAATACTCAG TTGATGTTCC 2280
AGAGGTTTAA AACAGAAAAA CTTACTTTAA AAAGGACAAA AATGACACTT TTTCAAATTT 2340
GATATTAACA TGAGAATTCA AACAGTAGTG TAAGAAGATG TACAAGAGTC TAAAGATTTG 2400
AAAGAAGAAT GATTGGAAGT GACGCAGTTA GAGCAGGCCT AACTGAACCA GAACGATGCA 2460
ACTCCACAGC TCCTCCCCTC CCCATTCCAG TGGAGCCAAC CCCACAGAGG GAATGGGAAG 2520
CACTCCCACA GGGCAACGTT TTTAACAGAA ATATATAACA ACTTTTGCTT TCAAAGTTGG 2580
GTGGGACTAG AACACACAAT GGAAGGATGG AGTCAGGAGA CCTGGATTCT TGTGCCCGCT 2640
CTGGCTTTTA CAGTCTGCCT AACTCTATGC AGTCACTTCC TGCCAGCCTG TTTCCTTACC 2700
TACAAGAGGG AGAGACACTC CCTGGCCAGC CTAGTTCTCA GGGTGAACGA AAGGTCATTA 2760
TCACTGCATC CTCTAGTCAT TTGCTTCTTC GCTAATTAAC ACATCTTGAG CACCTGCGAT 2820
GTTCCAGGAA CAGGAGATGG CAGCGTGCAA GATAAAGTCC CTGACTTCTA GAGACTGCAT 2880
GTTAGTGGCA ATCGGCGTCT ACCCGGCCTT CAATAAACTA CTGAATGAAG GAAAATTCTA 2940
CCTAGCACCA GACACAATTA CTGGGTTTCT AAAATGGAAT TATTCCCCCG GCCCCCTGCA 3000
TCCAGCAGCC TGCTGCAGGG AAGCTCCTCC GAAGGCTGTA GGCAGGAGCG GGACAATGCT 3060
TGCTATCAGC TCCACAGATG TTACCTAGTA CTATTCCTAC ACAGCGCCTT ACAGAACAAA 3120
CAGTAAAACC AAGTGGAAAG CATGCACGGG CTTAAAAACT CAAACTCCTT AACTACTCAG 3180
TAATTAGGAT GTCATTTTAC ACCAAAAATA GATTTTTCTA TTTTATACAA TAGAAGGAAA 3240
GAAATGTAGT GCAGAGTGAG TCATTAGATC GTGACCTTAT ACTGTCTTCA TCTCTGAATC 3300
TCAGACGCTG TGCAAAGCAG GGGGTCAGCA TGTGTTTGCT GAATGAGTAA CACTGTTCCT 3360
GTCAACAGGA ATACGGATTA CACCAGGTAG CTCTCAAACT TCCTCCTCAA TCCACTCCTC 3420
CTTTTACATT CATGGAAAGG GAGGGGGAAA GAAGCCCAGT CTCCAAGGTC AGCCAGTTAC 3480
ACCAGAAGCA GTGCCACCAG AATATGAGCC CCGCCCTGGG ACAGGGCACA GAGCCCTCAC 3540
TAGCATGCTG GAGAGGGGCC ACCCCAGGTC CTGGGTTTCC CTATACCCAG CTGCTTCTCT 3600
TCAAGCTGGT GAAGCCCCTG CCACCGCCAC CACCTCCTCC CCTACCTTGG GACTTTGTGT 3660
TTAATCCCGG AAGTCACAAT TTAGGAGGCT CAAAAAGAAT AAAATTCTGG GTATACAAAT 3720
GGAAAAGACC CAAATGTGTC TGTCAAGAAT AGCCAAAGGG ATGGGATTAT TTAGCCAGGA 3780
GAGGCTGTGG GAGGGATGAT GGGTGAAGTA CTTGAGATTC TTGCTATTTT TCTAACAGTT 3840
TTATTAAGAT AATAATTCAC ACAGTTCACC CATCTAAAAT GTACACAATG ATTTTTAGTG 3900
TGTTCACAGA GTTGTGCCAC ATCATGACAA TCATTTTAGA ACATTTTCAT CACCCCAAAA 3960
AGAAACCCCA CACCCTTCCC CAGTCATCCC CCACCTCCTC TACTCCCAAT CCTGGCAATC 4020
ACTAATCTAC TTTCTGTCTC TATGGATTTG CCTATGCTGG ACATTTCAGA TAAATGGGAT 4080
CATAACATGT GGCTCTGGTG ATTGGCTTCC TTCACTTTTT CCAGAATGTC 4130