EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-04509 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr10:73733960-73736580 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs116508194chr1073734991hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr10:73736042-73736053GGTGACTCATT+6.02
STAT3MA0144.2chr10:73736222-73736233TTTCTGGGAAG+6.02
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00376chr10:73733343-73737385Adipose_Nuclei
SE_00890chr10:73731831-73736604Adrenal_Gland
SE_01702chr10:73729991-73737296Aorta
SE_03170chr10:73732394-73737370Brain_Angular_Gyrus
SE_03943chr10:73728232-73743563Brain_Anterior_Caudate
SE_04798chr10:73727845-73748768Brain_Cingulate_Gyrus
SE_05790chr10:73728054-73748631Brain_Hippocampus_Middle
SE_06730chr10:73728098-73748557Brain_Hippocampus_Middle_150
SE_07761chr10:73727829-73748603Brain_Inferior_Temporal_Lobe
SE_08800chr10:73734310-73734608Brain_Mid_Frontal_Lobe
SE_08800chr10:73735578-73736461Brain_Mid_Frontal_Lobe
SE_26189chr10:73734320-73736894Duodenum_Smooth_Muscle
SE_26917chr10:73733879-73737221Esophagus
SE_29757chr10:73733093-73736918Fetal_Muscle
SE_31814chr10:73734002-73736629Gastric
SE_36082chr10:73733043-73737393HMEC
SE_36975chr10:73727846-73743322HSMMtube
SE_40893chr10:73733166-73737429Left_Ventricle
SE_42457chr10:73733902-73737400Lung
SE_44314chr10:73733057-73737142NHDF-Ad
SE_46483chr10:73733139-73737520Osteoblasts
SE_46661chr10:73734111-73736467Ovary
SE_47649chr10:73734342-73734843Pancreas
SE_47649chr10:73735231-73736398Pancreas
SE_48621chr10:73729126-73737386Right_Atrium
SE_51872chr10:73733055-73737228Skeletal_Muscle_Myoblast
SE_54185chr10:73734364-73736645Spleen
SE_54706chr10:73734189-73737661Stomach_Smooth_Muscle
SE_63666chr10:73729615-73737242HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr107373402373736528
Enhancer Sequence
ATCATAGAGG CCCTTGAATG TCATTCTTTC CATTCACTAA GCACCTGCCA TGTGCCAGAT 60
TCTTCACAGT CATTCTCACC AAGCCCCCTA CAACCCGGCA AGGTTGTTAG CAATGTCTCC 120
ATTTCACAGA TGAGGAAACT GAGGCTCAGA GAGGTTGAGT AACCTGCCTA AAGTCACTCA 180
GTCAGGGAGA GTCAGAGCCA GTAATAACAC CCAGGTCTGC TGTCGCTTGA GTCTTCCCTC 240
AAAGTGAAGA TTGGAGAGAC ATGGCAGGGG CATCACAGGG ATGAGCCCTG GGCTGGGGCC 300
GCAGCCAGGA GCAGAGCAGG AATGTGGCAA CTGTGGGTCC CTGGGGCAGG GTGGAGACGG 360
GGAGAGATGC CAGGCGGGCC TGGAGGGTAG GGAGGACTGG AGGCTACAGC ATACAGCTCA 420
CCATTCATAG CCCAGGGCAA ACCATTGAGT CATTTGGGGA AAACATGACA TCACTGAGTC 480
TCACTGTCTG CCGCCCACCT GCTGTCTGCC CTCTATGGTT CTCCTGATGA CCTCAGTGCC 540
CCAAGTCCTG CAAGGGGACC CGCACACCCC ATGTAGCAGG GCCAGGTCAG CACTCCAGCT 600
TCCTGCACTG GGTTCTCCTC CCCAGCCACT GTCTCCCACC TTCCCACCAC TCCCTTCCCT 660
GCCTGGGTCC CCTGCCCCAG CCCTACTCAT ACACACTGCT GAGGCAGAAG CTTCTGGAAG 720
TGGTGATGGG CATGAAGAGC TTCCAGAAGG GCTTCCATGC CAAGCCCTTG ATTGGAATTC 780
TGGGTGGGGA GGGGACAGCT CAGAAGCCTG TGTCGAGCTT TTAGAGTTGC TTTTCCTTGA 840
GAATGGTGCC TGCTGTTTGG GTGGGATCAC TTTTAAAAAG TAAAGCCTGG TAGAGCTATG 900
TGACCAGCAC TATGCCATGA CCTAGAGGAG ATTCAGACTG ACGGGCAGGC CCTGCCTTCC 960
TGCAGAATAC AGTTGAGTGT CTGAGAGTTC TTTCTGTACT AAGCATCTTT GAACTGAGTG 1020
CTTTATTTTC GTCCATCTGA TTGCGCGAGG TAGTCTTATT TTACAGATGC CATCCCCGAG 1080
GCCCAGAGAG GTTAGGCAAC TTGTCCAAGG CCACACAGCC AGGATTCACA CCCATAACTG 1140
TCCAACTCCA GATGTGCTCT TAGCCACTCT GCCATCCGGC CACAAATAAA GCCACCAGAG 1200
AACCACAGAA GGTGGAACAT ATCCAACATT TGCCCGATAA ATTGTATAGT GCAGACAGGA 1260
AGTACAGGGA GTTTTCATCT CAAAGTGTAG GTCACTCCCC AGAGTGGCTT GAAGTCTGTA 1320
GATCCATTTA GGAGAACATC CAGCTTCACT GGCTGTGCAA ATCCCACCCA TGCGGCTGTT 1380
TGGGGTGAGA AGTTTCTTTA AATGTCTGTT GACTCTCTTC TCTGGAAGGA GCACGGGGGC 1440
TCAGGGGGCG CCTGTCCTGG CATTGGTGGC CACACCTAGA AACGGACTAT GAATCAAGCC 1500
AGGGGCCCAG TGCCAGCTTC CTTGGCCTGT CTGTGGGCGC AGATGCCAGC CTTTGCAGCT 1560
GCTGCTGCAA CTCACAGCTC TCTCCCGGTG CCGCCCTCAG TCAGGCCAGC TGGAGTGGAG 1620
GGGCCAGTGG CCGTGCCCTG TGCAGAATGA CATCCTCTCA CCTTCACAAG GGAAGCGTGA 1680
TTATCCTTGC TTTCCAGGTG AGGACACTGA GGCCTAGAGA AGTTTTCTGG CTGTCTGAGC 1740
TCCCTTGGCC TGAGCTCCCG CGGTAGAACC GAGACTCAAG TCTTCTTTCT GCAGGCAGAT 1800
GGCCAGTTTC TTCCTGGAGG AGGGAGGAGC CAGCTTGCCC TCTGACACTG GGTAGCACAG 1860
CCCTGTTCGA TTCTCTGTTC GGGGCTTGCA CTTCTGATTC ATTCTGCAGT CACTGGCTCT 1920
TTGTGGTTCG GGAAAATGAC CCTCTAGGGT AGGAGAAAAG CTCTTGGAGC ACTTTTGAAG 1980
CCATAGAGGC CCTTTCCAGG CTTTGGAAAA TGTTCCTTCT CCACCCAGAT GCCAACACCA 2040
CCCTGGTCCT GGCAGTACTT GTCCCTGGAA GGGCCTCACT GCGGTGACTC ATTACCCAGC 2100
ATGCAGCACA TTGCCATTGC TCTCAGTGGG CAGGTGCTGT GGGGACACGG GTCTGCGGGC 2160
CTGCTGTCTT CAGGGGTCCC CCATGCCTTT TAACGCGTGT ATCAGTGTAC CCCAAGCCTC 2220
AGTTCTGTGT AGTTTGTACA ACTCTGGCCC CTACCCCAAG GATTTCTGGG AAGCCCCCAG 2280
GAATGCTGAT AAGTTCACAG TCTGCCCTCC CCAGCCCCAG TCTCATCAGG CTTCAGGGGT 2340
GGCCATTCCT CCCCTCCAGG AGAGAGAGAA CTCAAACCAG TAACTACCCC TCCTCAGGCT 2400
CAGGCCCAAT GGTTGCTGTA ATAATTTCTG GGGAGCTGTC TTTGCTCTTG CAGAGAAGGC 2460
AGGCCTTGAA TTCAGACTGG AGGGGCCATT TTTCTTCCAG TTGCCCTCAA ATTTTCCTTT 2520
CTGTGATAGG ATTTGTCCTT TGTCTCTGCT TAAATTCAAA GACTTGTTAA AATGACTTTT 2580
CTCAAACAAG AGGCTACCCT CAAAAGAACT TTGCCTCTAC 2620