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

TagContent
EnhancerAtlas ID
HS051-06747 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr12:111881980-111884450 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr12:111882363-111882376AGCAGCTGTTGCT+6.59
PLAG1MA0163.1chr12:111883832-111883846GGGGCCCAGTGGGG+6.36
ZNF263MA0528.1chr12:111882477-111882498CTCCCCTCTCACCCATCCCCC-6.17
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
SE_00313chr12:111877184-111889811Adipose_Nuclei
SE_01105chr12:111882374-111885128Adrenal_Gland
SE_03792chr12:111882112-111882730Brain_Angular_Gyrus
SE_03792chr12:111882777-111884396Brain_Angular_Gyrus
SE_06099chr12:111881910-111889732Brain_Hippocampus_Middle
SE_08462chr12:111882037-111889880Brain_Inferior_Temporal_Lobe
SE_09337chr12:111861899-111889874CD14
SE_11164chr12:111877342-111885335CD20
SE_11924chr12:111881996-111883985CD3
SE_13643chr12:111879661-111884327CD34_Primary_RO01536
SE_14612chr12:111881982-111884743CD4_Memory_Primary_7pool
SE_15617chr12:111882237-111883985CD4_Memory_Primary_8pool
SE_16453chr12:111881793-111883917CD4_Naive_Primary_8pool
SE_17009chr12:111881890-111884352CD4p_CD225int_CD127p_Tmem
SE_17538chr12:111879408-111885017CD4p_CD25-_CD45RAp_Naive
SE_17816chr12:111879397-111885095CD4p_CD25-_CD45ROp_Memory
SE_18496chr12:111878855-111885074CD4p_CD25-_Il17-_PMAstim_Th
SE_19231chr12:111879894-111884513CD4p_CD25-_Il17p_PMAstim_Th17
SE_20028chr12:111881146-111884553CD56
SE_21344chr12:111881937-111883925CD8_Memory_7pool
SE_22364chr12:111881633-111884909CD8_primiary
SE_24616chr12:111882262-111885111Colon_Crypt_2
SE_32074chr12:111882081-111884569Gastric
SE_38040chr12:111879609-111885412HUVEC
SE_40792chr12:111877378-111887912Left_Ventricle
SE_42263chr12:111881886-111887837Lung
SE_46057chr12:111881866-111884857Osteoblasts
SE_47422chr12:111880472-111884943Panc1
SE_48851chr12:111882225-111887877Right_Atrium
SE_50268chr12:111881894-111887773Sigmoid_Colon
SE_52677chr12:111881995-111885302Small_Intestine
SE_53326chr12:111877253-111887851Spleen
SE_62745chr12:111834432-111886877Tonsil
SE_68830chr12:111882255-111885010H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12111882042111883715
Enhancer Sequence
AGAGTGAGAA TCTGTCTCAA AAAACAAAAA CAAAAACAAA AAACCCTAGA GGATAAAAGA 60
ACTATAACAT CTGGGATAAA GTTAGCTGTT GAAATAAATA CAAGTCCTAC CGTTGGGGTA 120
GTGTCAGAGC TGGCCTACGT CTTTGACTTT GAGATTCCTA GCAGCCAGAG CAAAGAAAGA 180
AATAGATTAT TCCCACTGGA GCCACAGTGG CCATAACAAA CAGAAGCCAT CTGTTTAGAT 240
GCTGGGAATG GAGAAGACTT GCTCCCCAGA AATAGACGCT GCAGGATGTG GTGGGTGACA 300
GTCTACTGTT CAAACCACAA ATACCTGAAA TGATCTGGCC ACTTTGATCA CCCAACCACA 360
GTAGAGCCTA AGCAGGTCCA GGGAGCAGCT GTTGCTGGCC TGGCTTGACT TTTGAGGGAG 420
GTGGAATAGC GGGCATGTGA GAGGAGGGAA CCTAAAGCCC CCACAGCTGC TGACACAGCC 480
CCCAGGTTTG AGCTTGTCTC CCCTCTCACC CATCCCCCCA TATAGCTTAA TCTGATGGGC 540
ATCTGGTGGT CCTTCCCTGC AGTGGCCAGA GCCTGAGCTG TCCAGGCTGA GGTTTCGACT 600
GAAGCAGGGG TTGTCCTGCG CCCATGTGCC CACACGCTGC AACCTGGCTG GAGCCTCTGG 660
CATAGGACAC CCATACCACC AGGTAGCTGT GGCGGACCCC GGCTCTGATA CTTGGCAGGC 720
TTGGGTTGAG ATTGTGGCTC TAGGCCTGGG CGGCTCTCAA GGGCTGCTGT GGGGAGTTGG 780
GGAAGAACCC CTGGGTTGTG CTCAGCCAGC AGGCAGGTGG CAGCCAGGCT GGCTGTGGGT 840
GAGGAGGGGA ATCCTCTTTT CACCACTGCC TGCCTGCTCA GCAGTTCTTC AGCTGCTGGG 900
GGTGGAGCTG GCTTGCAGGG GCCAGAGTCA GAGTGAAACC GGCAGCTCTG CTGGTTAATC 960
TCAGCACTGA CACTGGGGAC TAGGCCTGGA GCGGAACTGA AAGGGAGACT AGGCCCGTTC 1020
CCCTCCAGGC CTGGCCTATA TCCTCCCAGT GATCCTTAAG GCCTGCAGCT AGGGGGAAGG 1080
GTGGGGGCCA GGCAGGGCCA ACTGGAAAAG TAGCAGAAGG AAGTGGCCAC TCGCACCTTA 1140
CCCATCTTGC AGACAGGAAA TGAAGGCTCT GCAGGGCTGG CTGGCTGTAA AAATGGGCAA 1200
GAGCGCAGAG GCCCCACTCC CTGCACACTG CGCTGTGTCC AGTGCCCGTG TGGATGCCAT 1260
GTGAGGCCTC ACTCTGCCTG CCTCATCCTG GCTGCTGGAC CTCTGGGAGT AGGAGGTGAA 1320
AATGCCCTGG CTGGTGCTGG TCACTTCAGG CTGGAATTTT CTAGTCATGC AGCTTTCTAG 1380
TGAGAGGCCG CAGTGAGCTG TGGCCAGTGT TGGTCATTCC TGCAGTCATT ACTCTCCCCC 1440
AGCCTGTTGT GTCCGCCAAC CAGAGCAGGC CCGGGAGCTC CCAGGAGACC TGCTGGAAGG 1500
GCCCAGGTGG CCATCCTGCT CCTGCCAGGC TGCCCTCTTA CCTCACTGTT CATTGACTCT 1560
CCTGCAGGTG GGGAAGGGGG ATAAAGGAGG TGGCCAGGCC ACTGGGTCAT GATCCTTCCG 1620
ACAGAGGTAC CTGGCAGCTC TGTGTGTAAA GCAAGGTTAA GCATCTGGTT TTGGGGGTCA 1680
ATTCAACAGC ACTAGCAGCT CCAGTCCAAG GTATGCCCTT TTGGGCTGAG GTGGAGGTCA 1740
GATCACCTGA AGCCACAGTT GCTAGAACAT CCTTTGGGCT GCCTCTGCTT TCCATCCCCC 1800
TGCTCCCAGT TTGTTAGGGG TTGTAGTATT TTCCAGGAAC ACCTGAATGG AGGGGGCCCA 1860
GTGGGGCCAC TTCTGTCCAT TCCTTATCTC ATCTCTTTCT CCCCTTTTCT TCTTTCGGCC 1920
ATCTTTTCAG TCTTATCACA AGAGGAAGGG GAGGGGCAAA CCCCCTCCTG AGCAGATTCC 1980
CAACCGGAAG CAGCTGGCTC CTTGGCTGCA GAGTGCCCCA GCACAGGAAG CATCTGCAGG 2040
GTCAGTTGAG ACCTGGGAGC AGGTTTCCTG CTGGCAAAGG AACAGTGGCT AACTCCTATC 2100
CACCCTGCAG CCCTATGTGC CGGGTGTCCT GGGAAGGTCC AGGGCCAAGA TTTTGTGGTT 2160
TTACAGTGGC TATAACTTAG GCTAGCCATG CTAGGCTCTG CCCCTTTGGG CTTGGTGTGA 2220
TGAGACCGTC AGCAGCTGCT ATCACCTGGC TGGGCAGGGA GCTGTTTGCT CACCAGTGGG 2280
AAGAGAAACG GATGTCAGAC ACATGGCAGA GTGGGAATGT CTCCAAGTCC AGGTCCAATG 2340
GGCTGGGAGG GCTGGCCTTC TGCCAGCACA TGCTTCTTGG GATCTCAGTG TGAATGGTGT 2400
TCAGGAGGCT AGGGGAAGGC ACCCTGGACC TCACTACAGG CTCAGAGCCT GCCCAGCAAC 2460
ACCATGGATA 2470