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

TagContent
EnhancerAtlas ID
HS041-05759 
Organism
Homo sapiens 
Tissue/cell
EWS502 
Coordinate
chr12:123372950-123374700 
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_03969chr12:123372158-123374142Brain_Anterior_Caudate
SE_04866chr12:123372627-123374025Brain_Cingulate_Gyrus
SE_05835chr12:123372506-123374335Brain_Hippocampus_Middle
SE_06752chr12:123372427-123374364Brain_Hippocampus_Middle_150
SE_07820chr12:123371511-123373975Brain_Inferior_Temporal_Lobe
SE_11355chr12:123370263-123387549CD20
SE_12882chr12:123371153-123375031CD34_Primary_RO01480
SE_13364chr12:123370352-123377384CD34_Primary_RO01536
SE_14078chr12:123370527-123374122CD34_Primary_RO01549
SE_14078chr12:123374135-123377388CD34_Primary_RO01549
SE_15159chr12:123371489-123374216CD4_Memory_Primary_7pool
SE_20678chr12:123371452-123375661CD56
SE_23035chr12:123371451-123374116CD8_primiary
SE_23035chr12:123374193-123375063CD8_primiary
SE_23125chr12:123371398-123374057Colon_Crypt_1
SE_23125chr12:123374210-123374794Colon_Crypt_1
SE_23796chr12:123371617-123374038Colon_Crypt_2
SE_23796chr12:123374267-123374702Colon_Crypt_2
SE_25026chr12:123371394-123374077Colon_Crypt_3
SE_26757chr12:123370440-123374088Esophagus
SE_26757chr12:123374175-123382269Esophagus
SE_28186chr12:123370530-123374306Fetal_Intestine
SE_29262chr12:123370485-123374291Fetal_Intestine_Large
SE_30119chr12:123371598-123374763Fetal_Muscle
SE_31427chr12:123371483-123374784Gastric
SE_35883chr12:123370374-123381488HMEC
SE_37349chr12:123370777-123381030HSMMtube
SE_40937chr12:123371444-123374123Left_Ventricle
SE_40937chr12:123374195-123374891Left_Ventricle
SE_42306chr12:123371472-123374890Lung
SE_43888chr12:123371004-123381065MM1S
SE_47190chr12:123370007-123381847Panc1
SE_47585chr12:123372855-123374043Pancreas
SE_47585chr12:123374271-123374686Pancreas
SE_49030chr12:123372717-123374100Right_Atrium
SE_50159chr12:123371388-123374104Sigmoid_Colon
SE_50159chr12:123374182-123374874Sigmoid_Colon
SE_52477chr12:123370694-123374096Small_Intestine
SE_52477chr12:123374179-123374760Small_Intestine
SE_53586chr12:123371348-123374988Spleen
SE_61538chr12:123340041-123395084Toledo
SE_62830chr12:123354785-123387061Tonsil
SE_64309chr12:123370452-123374999NHEK
SE_65302chr12:123370430-123374818Pancreatic_islets
SE_66800chr12:123370544-123374097Jurkat
SE_66800chr12:123374223-123374829Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr12123374277123374697
chr12123373600123374131
chr12123374260123374548
Enhancer Sequence
CACAGCTGGG GAAGGAAATA AACCAACGAG AACTCTTGTC TCAGCATGTT CTGAGCGCCA 60
GTGATTACCT ACGAGTGGCT GGCACACGGT CTTCTAGATC ACCTCCCACT GCGTACCTGG 120
CATGAATCTC CATAGCAACA TTCTGCTACA AATACTGTAA TCAAAGCCAA ACAGGCAACA 180
AGGCCGGCAT TCCTCAGCTC AAGAACACAA CCACTCTGCA TACGACCGAC CGGTGAGGGT 240
CAAACAGTGC AGTCTACTTC TGGGTTCCTC TTCCAGCCAG TCTCTAACAG GATGTTAGGT 300
CATCCAACTT GTTTCTCTCG TTTCTCCCCT CCCTTCGATG GCAGCTCTTT CCTTCTCCCA 360
ACCCACTAAT AGCTCCTAGT GGCCTTTCAA ACTTTTATAT TCTCCTTGAT TTCCACAAGC 420
ACTTGGAGGA GAGTGGCTTG AATTTCTGTC TCCAAGCAGA GCATTCACCC TGAGCTCCAG 480
AACCACACTC CAACTGCCTG CGGGACAAAG CCCTGCCCAT CCCTCATGCT CTGCCTAATC 540
CGGCCTCAAT GACTCCCTCC CTCCTGCACC CCCACTGCCC CTCCCCTCCC CGCTCACCAG 600
AGCCCTGTCT CCTACTCACT TCCACTTGAA GCCCGGTTAT CACCACTCAC TCAGCAGCAC 660
TACCCAGGCA CATCCTGGGT GCCAGGCACT GTGCTGGGTG CCAAGGACAA AAAGACAAAC 720
ATGACAAAAT GCAGCCCCCA AGCCAGTGGG GGACACAGGG AAGTGACTTA CAAAATGTGT 780
GTCAAGTGCC ACAGGAGAGG TATACAAAGA AGCTAAGAGA CCACGTGCCT GTGACAGAGG 840
TGGGGAAAGC ACTTCAGGTC AGCAGGAGAG GGGAAGTGAG AAAGGGAGTC GGGCCAGCTG 900
GTCCGAATAC CTCTCCCAGA GCCCTAGCTC AAATCCTAAT TTCTTCCTAA CCTCCACTTC 960
CGCCGCCAAC CTGGTCCTGC CACGCCAAGC CAGCCCACGC TTTGCTGACA GATTAACCTC 1020
CCTAAAGAGC AGTTTCAGGC CGGGCGCGGT GGCTCACGCC TGTAATCCCA GCACTTTGGG 1080
AGGCCGAGGC GGACGGATCA CCTGAGGTCA GGAGTTCTAG ACCAGCCCGA CCAACATGGA 1140
GAAACCCCAT CTCTACTAAA AATACAAAAT TAGCCGAGCA TGGTGGCGCG TGCCTGTAAT 1200
CCCAGCTACT TGGGAGGCTG AGGCAGGAGA ATCGCTTGAA TCCGGGAGGC AGAGGTTGCG 1260
GTGAGCCGAG ATTGTGCCAT TGCACTCCAG CCTGGGAGAC AAGAGCAAAA CTCGGTCTCA 1320
AAAAAAAAAA AAAAAAAGAG CAGTTTCATC CGACTGCTTC TCTGCTCCAA AATCATCACG 1380
AAGCTCCTTG TTTCCTCCTA AATTAACCAC CATGGGGCGC ACACCCTGGC ACTCCCCCTC 1440
ACCAGCCCTA TTTCTTGTCA TTTCTCTACA CACAAGTACA TGCCATCTGG CCAAAGTAGA 1500
CGAGAACTCG CTCGTCGGAC AACCCATCCC TGCTTTCCTG CCTCTGTGCC TGTGTCACTT 1560
CCTCCTGAGC CCCCATTTTT GTCCATCAAA AGCCTACTTA GAGAAATAAA TAATTCACAA 1620
CAGTGGACAT GGGGAAGAGC ACACTGAGGG CAGAGCACAA GGCGGGGGGT TCCGCCGGTT 1680
GGCAGTGTTT ACTTCCTCGG CTGGGTAGCA GGTAGACAAA GTTCCTTATT CTCTGTGCCC 1740
TCTGGTAGAT 1750