EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS117-02752 
Organism
Homo sapiens 
Tissue/cell
LHCN-M2 
Coordinate
chr16:70739890-70741810 
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
GCCCAACCAC CCCAAGAACC CTATCGGGTT CTTCATGCCT CTGCTTCTCC AGTCTGGCAC 60
CAGGACCCTC TGGTGGTGCT CATTTCCCAC CCCAGCAGGT CCAATTCTCT AGCCCCACTG 120
GCCTGGTGGG GACCCTGCCT GCAAGCCCAG CTCTTTGGTC AGAGGGTGTC ATGGGGCATG 180
GGGTCAGCGA TCGCTGTGCT CCCTGGCAGG CTGTTGGCAG CTGTGGATGG GGATGGGGTT 240
CTTACATGGG TGACTGGGCA GGTAGTCCTG GCTCCAGGTC CCTCAGAGGC TGGGCTGGAT 300
GCTGATTCTG AGGACAGTGT GGGCTGGGTG GACTCCACCG GTCTCTCTGC AAGTCGCCTT 360
AGGACTGGGC AAACCAGCAG GAGGGCAACA GGCTTCAGGT GCCTGCTGAG GGCAGGGCAT 420
CCTGGCTCAG AGGCCCCTCC CTTCTCCCTA TGGCCAGGCC TCCTTCCTTC ATTTCCATCC 480
CCAGCTGCCT GTGGCTCACT GACCATGCAC AGAGGGGCGA GCCCTTGTTT ATTTTCTTTT 540
TTGAGACGGA ATCTTGCTCT GTCACCCAGG CTGGAGTGCC ATGGTGCGAT CTTAGCTCAC 600
TGCAACCTCT GCCTCCCGGG TTCAAGCGAT TCTCTTGCCT TGGTGGCTGG GATTACAGGC 660
ATGTGCCACG ATACTAGGCA CATTTTTCTA TTTTTAGTAG CGACATGTTG ACCAGGCTGG 720
TCTTGAACTC CTGACCTCAA GTGATCCACC CGCCTCGGCC TCCCTAAGTG CTGGGATTAC 780
AGGTGTGAAC CACCACGCCT GGATAGCCCT TGTTTCCTTT CTACATTGGA TGCTGGATGG 840
TGCCCACATC CATCCCCTTC AGTGGTCCAA GGCCAATGGA CCCCAGTACT TTCCTAGGAG 900
ACACCTGGAG TCTCACGGCC AATAAATCTG AGGTGCAACC TAATATCAAG GCTACAAACT 960
ACAGAGAAGG CCTGGACCGC TCCCACCGGA AAAGGGCCTC CTCCCTGCCT TGTTCCTGCC 1020
CCACAGCTGG GATCCTTTAG GAATTTAAAG AGAAAGCAGC TTTTGGGTCA GTATAACCTT 1080
AGGATAGGGA GAGGAGGGAG TAGCCTCCCA TCTCTAGTCC AGAACGCTCC AGAATCTCAC 1140
TGCATCCTGC CCCTCCCCCT CTGCTCTCTT CCCTTCCAAC TCTCTGCTTC CAAGTATGAA 1200
AACTGTAAAT CTGTTTTATT TATTTCAATC AATCCTCGGC AGTGTGCCCC TCAGGGCAAA 1260
GGCAGCCATG GTAACCCTGC CAACTCATGC CTTAAAAATT CATCGTTGTT TAATGCAGTC 1320
GATGTGTCTG GTACACTTAA AAGTTTCTTG CAGGGAGTGG GGTGGGAGGA GGAGGAGGAT 1380
GCGGAACTTG TTTTTCTGGG CTTTGTAGGG AGCTGGTGGA AAGGGGATGG AGGGAGGAGG 1440
GGCACAGGAA GAGGCCTTCA GTCCTCTTAG CCATCTGTCC CTCTGTGCAA GAGGAGGTGC 1500
CATCGGGCTC TGGGAGGTCC CAGACACCTG TGCTGGGCTC ATCTAGAGAC CTCCATAGAA 1560
GGTCTCATCT GGGTGGGAGC TGCCACAGAA AACGAAACAG TCTCACAGAG GCAGCTGAAG 1620
CCTCAGCCCC CCAGGATTAG CAGGTCCCTC ACCCTAAGTT TGGGGCTTGC TCTAGAGAGC 1680
AAGTTGACTC CCGCTTTCTG AACTGCCCAG GGTGGAGTCA GATGACCCTT GCTGCCACGG 1740
GAGGGGCTCT GCCTTCTCCT CAGAATGGAA GTCATCTTCT ACCTTGGCCC ATCGGGCTGG 1800
CTTGGCCTTT TTTCTTTTTT TTTTTTTCAA GATGGAGTCT CGCTCTGTCA TCCAGTGCAG 1860
TGGTGTGATC TTGGCTCGCT GCAACCTCTG CCTCCTGGGT TCAAGTGATT CTCCTGCCTC 1920