EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS036-01299 
Organism
Homo sapiens 
Tissue/cell
endometrioid_adenocarcinoma 
Coordinate
chr16:70739990-70741850 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4985417chr1670740642hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr16:70740347-70740365GCCTCCTTCCTTCATTTC-6.21
MEF2AMA0052.3chr16:70740576-70740588TCTATTTTTAGT-6.27
MEF2BMA0660.1chr16:70740576-70740588TCTATTTTTAGT-6.32
MEF2CMA0497.1chr16:70740575-70740590TTCTATTTTTAGTAG-6.57
Nr2f6(var.2)MA0728.1chr16:70740613-70740628TGAACTCCTGACCTC-6.22
ZNF263MA0528.1chr16:70741254-70741275GGAGGAGGAGGAGGATGCGGA+6.31
ZfxMA0146.2chr16:70740638-70740652CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_01571chr16:70730301-70741871Aorta
SE_05921chr16:70719888-70741838Brain_Hippocampus_Middle
SE_25984chr16:70740060-70741704Duodenum_Smooth_Muscle
SE_26579chr16:70730268-70741831Esophagus
SE_29572chr16:70741017-70743137Fetal_Muscle
SE_31075chr16:70740777-70744190Fetal_Thymus
SE_31605chr16:70740588-70741840Gastric
SE_33572chr16:70718442-70740384H2171
SE_33916chr16:70739621-70742446HCC1954
SE_36921chr16:70714857-70743663HSMMtube
SE_39037chr16:70739409-70742378IMR90
SE_42154chr16:70739975-70741871Lung
SE_44141chr16:70733445-70742522NHDF-Ad
SE_44759chr16:70739688-70741996NHLF
SE_46175chr16:70733960-70742039Osteoblasts
SE_46696chr16:70739517-70740438Ovary
SE_46696chr16:70740486-70741793Ovary
SE_50132chr16:70733513-70741853Sigmoid_Colon
SE_51796chr16:70740408-70741885Skeletal_Muscle_Myoblast
SE_52557chr16:70739936-70741816Small_Intestine
SE_53344chr16:70733802-70746442Spleen
SE_54517chr16:70733287-70742143Stomach_Smooth_Muscle
SE_55502chr16:70741229-70741826Thymus
SE_63572chr16:70732961-70740221HSMM
SE_63572chr16:70740308-70741996HSMM
SE_65255chr16:70720198-70742754Pancreatic_islets
SE_68272chr16:70718649-70750960TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr167074080870741433
Enhancer Sequence
CCAATTCTCT AGCCCCACTG GCCTGGTGGG GACCCTGCCT GCAAGCCCAG CTCTTTGGTC 60
AGAGGGTGTC ATGGGGCATG GGGTCAGCGA TCGCTGTGCT CCCTGGCAGG CTGTTGGCAG 120
CTGTGGATGG GGATGGGGTT CTTACATGGG TGACTGGGCA GGTAGTCCTG GCTCCAGGTC 180
CCTCAGAGGC TGGGCTGGAT GCTGATTCTG AGGACAGTGT GGGCTGGGTG GACTCCACCG 240
GTCTCTCTGC AAGTCGCCTT AGGACTGGGC AAACCAGCAG GAGGGCAACA GGCTTCAGGT 300
GCCTGCTGAG GGCAGGGCAT CCTGGCTCAG AGGCCCCTCC CTTCTCCCTA TGGCCAGGCC 360
TCCTTCCTTC ATTTCCATCC CCAGCTGCCT GTGGCTCACT GACCATGCAC AGAGGGGCGA 420
GCCCTTGTTT ATTTTCTTTT TTGAGACGGA ATCTTGCTCT GTCACCCAGG CTGGAGTGCC 480
ATGGTGCGAT CTTAGCTCAC TGCAACCTCT GCCTCCCGGG TTCAAGCGAT TCTCTTGCCT 540
TGGTGGCTGG GATTACAGGC ATGTGCCACG ATACTAGGCA CATTTTTCTA TTTTTAGTAG 600
CGACATGTTG ACCAGGCTGG TCTTGAACTC CTGACCTCAA GTGATCCACC CGCCTCGGCC 660
TCCCTAAGTG CTGGGATTAC AGGTGTGAAC CACCACGCCT GGATAGCCCT TGTTTCCTTT 720
CTACATTGGA TGCTGGATGG TGCCCACATC CATCCCCTTC AGTGGTCCAA GGCCAATGGA 780
CCCCAGTACT TTCCTAGGAG ACACCTGGAG TCTCACGGCC AATAAATCTG AGGTGCAACC 840
TAATATCAAG GCTACAAACT ACAGAGAAGG CCTGGACCGC TCCCACCGGA AAAGGGCCTC 900
CTCCCTGCCT TGTTCCTGCC CCACAGCTGG GATCCTTTAG GAATTTAAAG AGAAAGCAGC 960
TTTTGGGTCA GTATAACCTT AGGATAGGGA GAGGAGGGAG TAGCCTCCCA TCTCTAGTCC 1020
AGAACGCTCC AGAATCTCAC TGCATCCTGC CCCTCCCCCT CTGCTCTCTT CCCTTCCAAC 1080
TCTCTGCTTC CAAGTATGAA AACTGTAAAT CTGTTTTATT TATTTCAATC AATCCTCGGC 1140
AGTGTGCCCC TCAGGGCAAA GGCAGCCATG GTAACCCTGC CAACTCATGC CTTAAAAATT 1200
CATCGTTGTT TAATGCAGTC GATGTGTCTG GTACACTTAA AAGTTTCTTG CAGGGAGTGG 1260
GGTGGGAGGA GGAGGAGGAT GCGGAACTTG TTTTTCTGGG CTTTGTAGGG AGCTGGTGGA 1320
AAGGGGATGG AGGGAGGAGG GGCACAGGAA GAGGCCTTCA GTCCTCTTAG CCATCTGTCC 1380
CTCTGTGCAA GAGGAGGTGC CATCGGGCTC TGGGAGGTCC CAGACACCTG TGCTGGGCTC 1440
ATCTAGAGAC CTCCATAGAA GGTCTCATCT GGGTGGGAGC TGCCACAGAA AACGAAACAG 1500
TCTCACAGAG GCAGCTGAAG CCTCAGCCCC CCAGGATTAG CAGGTCCCTC ACCCTAAGTT 1560
TGGGGCTTGC TCTAGAGAGC AAGTTGACTC CCGCTTTCTG AACTGCCCAG GGTGGAGTCA 1620
GATGACCCTT GCTGCCACGG GAGGGGCTCT GCCTTCTCCT CAGAATGGAA GTCATCTTCT 1680
ACCTTGGCCC ATCGGGCTGG CTTGGCCTTT TTTCTTTTTT TTTTTTTCAA GATGGAGTCT 1740
CGCTCTGTCA TCCAGTGCAG TGGTGTGATC TTGGCTCGCT GCAACCTCTG CCTCCTGGGT 1800
TCAAGTGATT CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA TTACAGGCGC CCGTCACCAC 1860