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

TagContent
EnhancerAtlas ID
HS105-21010 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr12:123355610-123357850 
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_01099chr12:123355360-123357245Adrenal_Gland
SE_03273chr12:123355465-123357273Brain_Angular_Gyrus
SE_03273chr12:123357373-123358247Brain_Angular_Gyrus
SE_03969chr12:123355116-123358789Brain_Anterior_Caudate
SE_04866chr12:123354237-123359304Brain_Cingulate_Gyrus
SE_05835chr12:123351481-123359219Brain_Hippocampus_Middle
SE_06752chr12:123354724-123358851Brain_Hippocampus_Middle_150
SE_07820chr12:123354601-123359255Brain_Inferior_Temporal_Lobe
SE_08837chr12:123356709-123357136Brain_Mid_Frontal_Lobe
SE_11355chr12:123352410-123359477CD20
SE_12882chr12:123354940-123357018CD34_Primary_RO01480
SE_13364chr12:123355283-123359366CD34_Primary_RO01536
SE_14078chr12:123355463-123357226CD34_Primary_RO01549
SE_15159chr12:123355584-123357276CD4_Memory_Primary_7pool
SE_23035chr12:123354594-123357509CD8_primiary
SE_23125chr12:123355398-123359005Colon_Crypt_1
SE_23796chr12:123355502-123357276Colon_Crypt_2
SE_23796chr12:123357343-123358454Colon_Crypt_2
SE_25026chr12:123355420-123358300Colon_Crypt_3
SE_26757chr12:123354675-123358275Esophagus
SE_28186chr12:123355056-123357781Fetal_Intestine
SE_29262chr12:123355173-123357938Fetal_Intestine_Large
SE_30119chr12:123355056-123358608Fetal_Muscle
SE_31427chr12:123343773-123359126Gastric
SE_35883chr12:123355746-123357484HMEC
SE_37349chr12:123354568-123359385HSMMtube
SE_40937chr12:123354579-123358546Left_Ventricle
SE_41807chr12:123355474-123358982LNCaP
SE_42306chr12:123354685-123359130Lung
SE_43888chr12:123355207-123358920MM1S
SE_47190chr12:123350856-123362813Panc1
SE_47585chr12:123355495-123357272Pancreas
SE_47585chr12:123357383-123358372Pancreas
SE_49030chr12:123355427-123358859Right_Atrium
SE_50159chr12:123355321-123359100Sigmoid_Colon
SE_52477chr12:123355272-123359011Small_Intestine
SE_53586chr12:123355323-123358542Spleen
SE_61538chr12:123340041-123395084Toledo
SE_62830chr12:123354785-123387061Tonsil
SE_64309chr12:123355434-123357699NHEK
SE_65302chr12:123355407-123357338Pancreatic_islets
SE_65302chr12:123357610-123358375Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12123357200123357778
chr12123356600123356790
Enhancer Sequence
GCAAGGAACA CACAAGATGA TGAGAACCAA AAGTATATCA GCTCCTAAAC CCCTGAGGTC 60
CCCACGCACA CCCCAGGAGC CCAGTGCAGC TGCTGCCACC TCACTGGTCT CCACAGCTGG 120
CACCGCATGC CAGGCAGATG CTACTGACCC AGAGCCAAGC CCCTTGGTTT CTCATTTGGA 180
GCTGCTGCCC GTCGTAAAGA ATGAGGCCGA CTTCCTTCCA GCACGTTTCC AGGACAGGCT 240
TTGTCCTGTG ACTCCATGCA GAGCCTTCCC TGCCACGGCT GCGCTGTGAC TTGAATTCCT 300
TACTACGGCC ATTGTGCTTG CAGAAGTAAA CAGCTGTAAA GATTTAGAAT CTGATTTTTT 360
TCAAAACAAG TTTCTGCTGC TCCCGAGGAA GTTAAGGAAT CACTTATCAG CAGGAGACCA 420
GTTGGCATGA TGTCAATTCA GGCTTCATAA GCAGGCTAAG AGGTCCAACC AGCAAGCTGA 480
AGAGACCCTG GGAAGGAACT GTGTTTCCAG CCACCGGGGT TCCTCTGTCT CTCCCATGCC 540
CACCCCAGCT CTTCTGAGCC TTCCAGCTCC TAGCTGTTGG TGGGTGAGCA AAGCCGACCA 600
AAAGCTGGGG GAAGAGGGGG GACATATTTT GCCCATCAGG GATTTCATTT TGTCCTTTAA 660
AGCAATGACA GGCTACCCTG GTAGGTAGAG AAGAAGCCAC ATGCCCAGAA CTTAGGGGAG 720
AACGACAGGA GTAGAAGGTC TGAGAAAAAA AGGCAAAACG CTCCTAGCAA AACTTAGCCA 780
AAGTTTAAAT AAAAAACACA AACGCGTGGG TACCCTAGTT CCCTTTTCAC TCACTGGTGA 840
TCGGCTTCCT CTACCACAGC CCAGCCGCCG CCACCTCACT TTCCTTCCAC ACCGTCAGTT 900
TCAACAGCAT GCGATTCCTT ACCCAGCGTG TGTCCCTGTT TCTCTTTAAG CAGCTCTTCT 960
TCAACGCCAC CCCAGTCATC TCATTTTCCC CTTAATATTT TCTACCACCC CACCCAGGCT 1020
ATTTTTGCTG CGACTTCCTT CCTCTTAGTA GCTCGAGTAT AGATTCCTGG CCATGCTGCC 1080
TCTGCTCCCC ACCCCCAGTC ATACCCGTTG ATTGCTGTCA TAGTTCCTGG TGCGCTCACA 1140
CGAGTGCACA CGCACCACAC ACACAAGGAA GAGCCTCAGG GAATCAGAGA ACAAAGAAAG 1200
AAGCCCTTGG ATCCATGCCT CAATCAGGAG ATCCCTAACC CCAGCAGGAG GGCTCTTTTC 1260
AGCAGACAGT GATCTGCATC TCCAGACAAC AGCTGCACCC AGGGCCCTAA AGATCAGGCT 1320
CTGCTGAAAC CCAACAGGAT TTAAATGACA ATGAAAACCA AACCTCTCTC CCAACTCTAA 1380
AGTAAAAGCT AGGAGTGTCC TCGAAATGTG GGTGGTAGAA ATGCTTTCAT CTCTTCTGAT 1440
GCCTTTAGCA AAAAAGGAGA ATCTTGGGAC TGGAAAGACG CAGTTTCACT CGGGTTTCTG 1500
GTAAGCAGTG GGGCTCCCGT CACCCGCTTC CCCACCCACA GGGCGGCTCT CCATGGGCTT 1560
TCTATGCCAG GCCATGCAGA AGCGTCTTTC CTTCCATTGT TAAGTCATTT AAAAGAACAA 1620
ACAAAAACCA CTGTATGGCC ACTCTGGAAA ACAGGCACTT TTTAATAAAG CTGAATACGT 1680
AACTACCCTA TGACCCAGAA GTTGTACTCT TGGGCATTTA TATCAGAGAA ATGAAAACTT 1740
ATATTCAACA AAAACCTGCT CAGGACTGTT GAGAGCAACA TTTATTTGTA ACAACTAAAA 1800
TCTGGACGCA GCCCAGGTGT CTTTTAACAG GTGAATGGTT AAACAAGCTG CAGGCCAGCC 1860
AGGCCGCAAA ATACCACTCA GCAGCAAAAG GAAGAAACTT GACTGGCGGG ACTGAGAACG 1920
CTCTAGGGAA TCACACTGAA GGAAAACAGC CAACCCCAAA GGGCCACTCA CTCCATGACC 1980
CCATGCACAC AACACCCTTG AAATACAAAA TCACAAAAAT AGAGAACAGA TTAGCGGTGT 2040
GTGTGGGACT ATAAAAGGCC GACATGACGG ATTTGCACGG GGACGGAGCC GTCCTGATGT 2100
TCTGTGTCCT GGCAGTATCA GTGCCCCGAT CCTGGTGCTG AGAGTGCGTT GAATTTCACC 2160
AGATGTTACC CAGGGGGCAG CTGGGAGAAG GGGACACAGG ATCTCTCTGT ATTCTTTCAA 2220
CTGCATGTGA AACTATGAGC 2240