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

TagContent
EnhancerAtlas ID
HS131-00198 
Organism
Homo sapiens 
Tissue/cell
ME-1 
Coordinate
chr1:27847720-27849100 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs59180873chr127848634hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:27847997-27848015CCCAGCTTCCTTCCTGCC-6.1
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00861chr1:27845422-27848562Adrenal_Gland
SE_01588chr1:27847229-27850959Aorta
SE_03261chr1:27846755-27848207Brain_Angular_Gyrus
SE_03261chr1:27848220-27851115Brain_Angular_Gyrus
SE_03939chr1:27845236-27851100Brain_Anterior_Caudate
SE_05196chr1:27845131-27856743Brain_Cingulate_Gyrus
SE_05814chr1:27844227-27851238Brain_Hippocampus_Middle
SE_06945chr1:27845183-27851030Brain_Hippocampus_Middle_150
SE_07770chr1:27844238-27856992Brain_Inferior_Temporal_Lobe
SE_08936chr1:27847787-27848068Brain_Mid_Frontal_Lobe
SE_08936chr1:27848269-27848780Brain_Mid_Frontal_Lobe
SE_14757chr1:27847180-27856512CD4_Memory_Primary_7pool
SE_23188chr1:27847642-27849034Colon_Crypt_1
SE_24033chr1:27847701-27848561Colon_Crypt_2
SE_24711chr1:27847113-27848532Colon_Crypt_3
SE_26518chr1:27843507-27857767Esophagus
SE_27625chr1:27843691-27857024Fetal_Intestine
SE_28547chr1:27843416-27856986Fetal_Intestine_Large
SE_29557chr1:27845136-27850991Fetal_Muscle
SE_31031chr1:27846218-27856799Fetal_Thymus
SE_31394chr1:27847672-27850831Gastric
SE_33477chr1:27843634-27857256H2171
SE_35950chr1:27847434-27851336HMEC
SE_36974chr1:27845141-27851091HSMMtube
SE_40593chr1:27844098-27856916Left_Ventricle
SE_42106chr1:27844182-27851151Lung
SE_48058chr1:27847224-27850904Psoas_Muscle
SE_48567chr1:27844222-27851412Right_Atrium
SE_49444chr1:27847670-27848476Right_Ventricle
SE_49444chr1:27848868-27849874Right_Ventricle
SE_50130chr1:27844122-27851113Sigmoid_Colon
SE_51091chr1:27846905-27847919Skeletal_Muscle
SE_51091chr1:27848905-27857215Skeletal_Muscle
SE_51984chr1:27847470-27849848Skeletal_Muscle_Myoblast
SE_52467chr1:27843721-27848576Small_Intestine
SE_52467chr1:27848710-27850530Small_Intestine
SE_54527chr1:27845490-27857100Stomach_Smooth_Muscle
SE_55184chr1:27847634-27851100Thymus
SE_62007chr1:27846487-27856737Toledo
SE_62718chr1:27801410-27856116Tonsil
SE_63223chr1:27848362-27856425GLC16
SE_63746chr1:27846637-27850471HSMM
SE_65253chr1:27843908-27851025Pancreatic_islets
SE_66890chr1:27843634-27857256H2171
SE_68682chr1:27848751-27850192H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr12784784327847948
chr12784818027848400
chr12784840027848542
Enhancer Sequence
CTAAGATTCC AGAGGGGAAG GGACTAGCCC GAGGCCACAG AGCACTGAAT TGGATGCAAG 60
GATTTGGACC TGGAGGAGTG TCCAGTCCAT ACTATCCACT TGCTGAAGGG GCAAATAGAG 120
CCAGAGAAGG GGAGCAAGTT CCCCAAGGTC ACTCCGTGAG TCTGGGGCCA GTGTGGGCCC 180
AGAGCCAGGC TGTGCACGAG GTCCCCTGCC CAGCTGCCTC GCTTGCTCAT CCAGCCCCCT 240
TGGTTTTGTC TCCCCCAGTG AGTGGGCGCA GAACGGGCCC AGCTTCCTTC CTGCCGCCCT 300
GCCTGCCGTC TGCCACGTTG GCATCCACCC TCAGCCTTCT CGCCCCTGCT GCTGCTGCTG 360
CTGATGCGGC ATCAGCCGAG ACCAACCCGC CGAGAGTTTG CCCAGAGCAG TCAGGGCTGC 420
CGGAGCCGGG GCTGGGCTGG CTGGCTGACT CTGCCAGACA GGAGGGAGCG AGCCAGCCGG 480
TGGAGGGAGG GAACAAGGGC TGAGCCAGCC CCCAGCCTTC CCAGCCCTTC CCCACCCTCG 540
CCGGCCAAGG GAAGGAGGCA GGAAGCTGGG GTTGGGGGCC AGGGGACTGC AGTGTCTGAG 600
AATGAGGTTC CGATAGCTGG GTCTGTCTGT GGGAGCATGC ACACATATGT GTGTGCATGG 660
AAGAGCACGT TGGGGTGGTT TGTGAGTCTG TGTTTGCCTC AATGTGCACA GGTGATGATG 720
CTATGTGTGT GGGTTTGTGC CGACATCGGG GGCCACTGTG TGTTTGTGTA AGCACAAGGG 780
AAAGCTGTAT GCCCTGAGTT TGAACGCAGG CCTGTGTACA GAGACGTGCG AGATCTAGCA 840
GTGTGTGCAC ATGGTAGCAG ATGGGCACCA CGTCAGTGCC AATAAATCTT TGTATGCACA 900
AAAGAGTCGG TACATGTGCC TGAGTTTGTG TATGTCACAT CTGGGTGTGT TGGGAGCCCC 960
TGTGATTTTA TGGTGTACAA GAGGATAACA GCATAACTGT GGGTTTGAGC TTGTCTGTGT 1020
ATGTGCAAGG GACAGTGTGT GTGCAGAAGG GAACTCTGCA GGTGGCTGGG ATTTTGTGCA 1080
TGTCTTGTGC CCAGGAAGGC ACAGTACTGG TGGTGTGGGC TAGTCCAAAT GTCCAGAGGA 1140
TGGGTATGGG CGCCTCTGTG CCCAACAGAC TTTGTCTGTG TGGTTGTTGA GAGTGACTCA 1200
GGGGAACACT GTGTGACTGT ATATGCTTGG CTGTGTGTAC AGGGAACAGG CAGCACAGGC 1260
ATTGTGTTTC TGTGGTTGCA TTTACACAGG GCGGTGGCGG CGGCGGTGGT GGTGATGGTG 1320
ACGGTGCTGT GCTACAGGTT TGCACTTGTT TCTCTATGTG GCAAGGCCCT GCGTGTGACT 1380