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

TagContent
EnhancerAtlas ID
HS183-01382 
Organism
Homo sapiens 
Tissue/cell
T47D-MTVL 
Coordinate
chr12:123372830-123374740 
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
CTAAGCTAAG TCACCTCTCT ACTTTCATTC TTCCCTTGGA AGAAATTCTA CAAAGGCATT 60
TCCTCTGCTT TTGTATCATT GGGTAAGACA TCATTTCCAA TGATGAAATC TGAAAACTCA 120
CACAGCTGGG GAAGGAAATA AACCAACGAG AACTCTTGTC TCAGCATGTT CTGAGCGCCA 180
GTGATTACCT ACGAGTGGCT GGCACACGGT CTTCTAGATC ACCTCCCACT GCGTACCTGG 240
CATGAATCTC CATAGCAACA TTCTGCTACA AATACTGTAA TCAAAGCCAA ACAGGCAACA 300
AGGCCGGCAT TCCTCAGCTC AAGAACACAA CCACTCTGCA TACGACCGAC CGGTGAGGGT 360
CAAACAGTGC AGTCTACTTC TGGGTTCCTC TTCCAGCCAG TCTCTAACAG GATGTTAGGT 420
CATCCAACTT GTTTCTCTCG TTTCTCCCCT CCCTTCGATG GCAGCTCTTT CCTTCTCCCA 480
ACCCACTAAT AGCTCCTAGT GGCCTTTCAA ACTTTTATAT TCTCCTTGAT TTCCACAAGC 540
ACTTGGAGGA GAGTGGCTTG AATTTCTGTC TCCAAGCAGA GCATTCACCC TGAGCTCCAG 600
AACCACACTC CAACTGCCTG CGGGACAAAG CCCTGCCCAT CCCTCATGCT CTGCCTAATC 660
CGGCCTCAAT GACTCCCTCC CTCCTGCACC CCCACTGCCC CTCCCCTCCC CGCTCACCAG 720
AGCCCTGTCT CCTACTCACT TCCACTTGAA GCCCGGTTAT CACCACTCAC TCAGCAGCAC 780
TACCCAGGCA CATCCTGGGT GCCAGGCACT GTGCTGGGTG CCAAGGACAA AAAGACAAAC 840
ATGACAAAAT GCAGCCCCCA AGCCAGTGGG GGACACAGGG AAGTGACTTA CAAAATGTGT 900
GTCAAGTGCC ACAGGAGAGG TATACAAAGA AGCTAAGAGA CCACGTGCCT GTGACAGAGG 960
TGGGGAAAGC ACTTCAGGTC AGCAGGAGAG GGGAAGTGAG AAAGGGAGTC GGGCCAGCTG 1020
GTCCGAATAC CTCTCCCAGA GCCCTAGCTC AAATCCTAAT TTCTTCCTAA CCTCCACTTC 1080
CGCCGCCAAC CTGGTCCTGC CACGCCAAGC CAGCCCACGC TTTGCTGACA GATTAACCTC 1140
CCTAAAGAGC AGTTTCAGGC CGGGCGCGGT GGCTCACGCC TGTAATCCCA GCACTTTGGG 1200
AGGCCGAGGC GGACGGATCA CCTGAGGTCA GGAGTTCTAG ACCAGCCCGA CCAACATGGA 1260
GAAACCCCAT CTCTACTAAA AATACAAAAT TAGCCGAGCA TGGTGGCGCG TGCCTGTAAT 1320
CCCAGCTACT TGGGAGGCTG AGGCAGGAGA ATCGCTTGAA TCCGGGAGGC AGAGGTTGCG 1380
GTGAGCCGAG ATTGTGCCAT TGCACTCCAG CCTGGGAGAC AAGAGCAAAA CTCGGTCTCA 1440
AAAAAAAAAA AAAAAAAGAG CAGTTTCATC CGACTGCTTC TCTGCTCCAA AATCATCACG 1500
AAGCTCCTTG TTTCCTCCTA AATTAACCAC CATGGGGCGC ACACCCTGGC ACTCCCCCTC 1560
ACCAGCCCTA TTTCTTGTCA TTTCTCTACA CACAAGTACA TGCCATCTGG CCAAAGTAGA 1620
CGAGAACTCG CTCGTCGGAC AACCCATCCC TGCTTTCCTG CCTCTGTGCC TGTGTCACTT 1680
CCTCCTGAGC CCCCATTTTT GTCCATCAAA AGCCTACTTA GAGAAATAAA TAATTCACAA 1740
CAGTGGACAT GGGGAAGAGC ACACTGAGGG CAGAGCACAA GGCGGGGGGT TCCGCCGGTT 1800
GGCAGTGTTT ACTTCCTCGG CTGGGTAGCA GGTAGACAAA GTTCCTTATT CTCTGTGCCC 1860
TCTGGTAGAT ATTATTCTAT TTAATAATTT ATTTTCTTAA CGTTTACCTA 1910