EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS129-14660 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr16:70739400-70742030 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4985417chr1670740642hg19
TF binding sites/motifs
Number: 8             
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
Nr2f6(var.2)MA0728.1chr16:70741912-70741927TGAACTCCTGACCTC-6.22
ZNF263MA0528.1chr16:70741254-70741275GGAGGAGGAGGAGGATGCGGA+6.31
ZfxMA0146.2chr16:70740638-70740652CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 28             
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_42154chr16:70733520-70739669Lung
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
GCAACCATCC CCTCCCAGGG GCCTCTGACA TTCTTGACTA TCCCAAACAA TAAGCCACCA 60
GCAGCGTGGA AAACAGCTGG CCTGGCGGGG ACAGACCCTG GACTCAAACC CTAGAAAGAG 120
ACAGCAAGGT TGAGAGATGA GCGTGGAGGC TGGGGGCGCC TGCTCCCGCC CGGCATGCCC 180
TCAGCTGCTC TCTCTACTCC AGCCCTCACT GGCCCCGCAA CGCTGCCCTC CCCATGATGA 240
ACAGAGGACT CAGAAGAAGC CTCAGCTGGC AAGTTCCAGG AGGGGTGGGT GTACCCCACC 300
TCCTCAGTTT TCCCCTATGC TCCACCTTGT CCACTCTCGC GTGCCATCGA TGGGACATCC 360
TTCCCAGTGG AGCCTTGTTG GTGGCCCCAT GAGAGGCAAG AGTGTGGGTG ATTTTGCTCG 420
GTACCTCCTG TTAGACTAGT TCACACAAGT GGCCTCACTG GATACAGATA CAGGAAGGTC 480
TCCTCCTACT GCCCAACCAC CCCAAGAACC CTATCGGGTT CTTCATGCCT CTGCTTCTCC 540
AGTCTGGCAC CAGGACCCTC TGGTGGTGCT CATTTCCCAC CCCAGCAGGT CCAATTCTCT 600
AGCCCCACTG GCCTGGTGGG GACCCTGCCT GCAAGCCCAG CTCTTTGGTC AGAGGGTGTC 660
ATGGGGCATG GGGTCAGCGA TCGCTGTGCT CCCTGGCAGG CTGTTGGCAG CTGTGGATGG 720
GGATGGGGTT CTTACATGGG TGACTGGGCA GGTAGTCCTG GCTCCAGGTC CCTCAGAGGC 780
TGGGCTGGAT GCTGATTCTG AGGACAGTGT GGGCTGGGTG GACTCCACCG GTCTCTCTGC 840
AAGTCGCCTT AGGACTGGGC AAACCAGCAG GAGGGCAACA GGCTTCAGGT GCCTGCTGAG 900
GGCAGGGCAT CCTGGCTCAG AGGCCCCTCC CTTCTCCCTA TGGCCAGGCC TCCTTCCTTC 960
ATTTCCATCC CCAGCTGCCT GTGGCTCACT GACCATGCAC AGAGGGGCGA GCCCTTGTTT 1020
ATTTTCTTTT TTGAGACGGA ATCTTGCTCT GTCACCCAGG CTGGAGTGCC ATGGTGCGAT 1080
CTTAGCTCAC TGCAACCTCT GCCTCCCGGG TTCAAGCGAT TCTCTTGCCT TGGTGGCTGG 1140
GATTACAGGC ATGTGCCACG ATACTAGGCA CATTTTTCTA TTTTTAGTAG CGACATGTTG 1200
ACCAGGCTGG TCTTGAACTC CTGACCTCAA GTGATCCACC CGCCTCGGCC TCCCTAAGTG 1260
CTGGGATTAC AGGTGTGAAC CACCACGCCT GGATAGCCCT TGTTTCCTTT CTACATTGGA 1320
TGCTGGATGG TGCCCACATC CATCCCCTTC AGTGGTCCAA GGCCAATGGA CCCCAGTACT 1380
TTCCTAGGAG ACACCTGGAG TCTCACGGCC AATAAATCTG AGGTGCAACC TAATATCAAG 1440
GCTACAAACT ACAGAGAAGG CCTGGACCGC TCCCACCGGA AAAGGGCCTC CTCCCTGCCT 1500
TGTTCCTGCC CCACAGCTGG GATCCTTTAG GAATTTAAAG AGAAAGCAGC TTTTGGGTCA 1560
GTATAACCTT AGGATAGGGA GAGGAGGGAG TAGCCTCCCA TCTCTAGTCC AGAACGCTCC 1620
AGAATCTCAC TGCATCCTGC CCCTCCCCCT CTGCTCTCTT CCCTTCCAAC TCTCTGCTTC 1680
CAAGTATGAA AACTGTAAAT CTGTTTTATT TATTTCAATC AATCCTCGGC AGTGTGCCCC 1740
TCAGGGCAAA GGCAGCCATG GTAACCCTGC CAACTCATGC CTTAAAAATT CATCGTTGTT 1800
TAATGCAGTC GATGTGTCTG GTACACTTAA AAGTTTCTTG CAGGGAGTGG GGTGGGAGGA 1860
GGAGGAGGAT GCGGAACTTG TTTTTCTGGG CTTTGTAGGG AGCTGGTGGA AAGGGGATGG 1920
AGGGAGGAGG GGCACAGGAA GAGGCCTTCA GTCCTCTTAG CCATCTGTCC CTCTGTGCAA 1980
GAGGAGGTGC CATCGGGCTC TGGGAGGTCC CAGACACCTG TGCTGGGCTC ATCTAGAGAC 2040
CTCCATAGAA GGTCTCATCT GGGTGGGAGC TGCCACAGAA AACGAAACAG TCTCACAGAG 2100
GCAGCTGAAG CCTCAGCCCC CCAGGATTAG CAGGTCCCTC ACCCTAAGTT TGGGGCTTGC 2160
TCTAGAGAGC AAGTTGACTC CCGCTTTCTG AACTGCCCAG GGTGGAGTCA GATGACCCTT 2220
GCTGCCACGG GAGGGGCTCT GCCTTCTCCT CAGAATGGAA GTCATCTTCT ACCTTGGCCC 2280
ATCGGGCTGG CTTGGCCTTT TTTCTTTTTT TTTTTTTCAA GATGGAGTCT CGCTCTGTCA 2340
TCCAGTGCAG TGGTGTGATC TTGGCTCGCT GCAACCTCTG CCTCCTGGGT TCAAGTGATT 2400
CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA TTACAGGCGC CCGTCACCAC ACCTGGCTAA 2460
TTTTTGTATT TTTAGTAGAG ACTGGGTTTC ACCATGTTGG CCAGGCTGGT CTTGAACTCC 2520
TGACCTCAGG TGATCTGCCG CTTTGGCCTT CCAAAGTGCT GGGATGACAG GCGTGAGCCA 2580
CCGCACCTGC CTTGGCCTTA TTTTCCATGT GTCTTTTCAG TCTGACCACC 2630