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

TagContent
EnhancerAtlas ID
HS139-25752 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr19:2064090-2066030 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2CMA0497.1chr19:2064382-2064397ATAATAAAAATAGAA+6.22
Nr2f6(var.2)MA0728.1chr19:2065976-2065991AAGGTCAGGAGTTCA+6.04
Nr2f6(var.2)MA0728.1chr19:2065686-2065701GAGGTCAGGAGTTCA+6.22
TEAD1MA0090.2chr19:2065585-2065595ATGGAATGTG-6.02
ZNF263MA0528.1chr19:2064467-2064488GGAGGAGCAGGCAGGGGAGGT+6.11
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00410chr19:2064401-2065846Adipose_Nuclei
SE_00877chr19:2064288-2066073Adrenal_Gland
SE_02925chr19:2064396-2065148Bladder
SE_03565chr19:2064465-2064959Brain_Angular_Gyrus
SE_04258chr19:2064386-2065787Brain_Anterior_Caudate
SE_05392chr19:2064123-2065842Brain_Cingulate_Gyrus
SE_06065chr19:2064093-2066049Brain_Hippocampus_Middle
SE_07327chr19:2064186-2065788Brain_Hippocampus_Middle_150
SE_08493chr19:2064398-2065926Brain_Inferior_Temporal_Lobe
SE_23148chr19:2064448-2065615Colon_Crypt_1
SE_23772chr19:2064682-2065031Colon_Crypt_2
SE_23772chr19:2065071-2065465Colon_Crypt_2
SE_26566chr19:2064282-2065665Esophagus
SE_28069chr19:2064386-2065634Fetal_Intestine
SE_28069chr19:2065744-2066861Fetal_Intestine
SE_29067chr19:2064373-2065439Fetal_Intestine_Large
SE_29067chr19:2065741-2068526Fetal_Intestine_Large
SE_29903chr19:2064127-2065780Fetal_Muscle
SE_31409chr19:2064310-2065685Gastric
SE_34292chr19:2064371-2065798HCT-116
SE_40728chr19:2063609-2065994Left_Ventricle
SE_42204chr19:2064122-2065796Lung
SE_46685chr19:2064438-2065103Ovary
SE_48086chr19:2055360-2066212Psoas_Muscle
SE_48699chr19:2063769-2065786Right_Atrium
SE_49469chr19:2064307-2065631Right_Ventricle
SE_50075chr19:2064365-2065787Sigmoid_Colon
SE_51187chr19:2063270-2066190Skeletal_Muscle
SE_52407chr19:2064329-2066217Small_Intestine
SE_59944chr19:2041147-2096724Ly4
SE_60429chr19:2041140-2096762DHL6
SE_65305chr19:2064032-2065820Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1920649802065181
chr1920647992065570
Number: 1             
IDChromosomeStartEnd
GH19I002064chr1920640272068184
Enhancer Sequence
GATGTTGACC AACACGTGTG TAAATGTTCA AGACCCACAT ATTTTAAAAA GTAAAAAGAA 60
ACAGATGACA TTGGCTGGGC ACAACATGGC CAACGTGGCC AAACCCCATC TCTACTAAAA 120
ATATAAATAT TAGCCGGGTG TGGTGGCACG CGCCTGTAAT CCCAACTACT CAGGAGGCTG 180
AGGCAGGAGA ATCACCTGAA CCCAGGAGGC GGTGGTTGCA GTGAGCCGAG ATCGCGCCAC 240
TGCACTCCAG CCTGGGTGAT GGAGCGAGAC TCCGTCTCAA AAATAAAATA AAATAATAAA 300
AATAGAATCT TAAAAATTGC CCGTCCTTCT GAGGCCTCCT GCACAGTCAT AGCGCCCTGT 360
GGCCCCGCGG CCAAGCGGGA GGAGCAGGCA GGGGAGGTTG CTTCCAGGAC GCCAGGACAC 420
TGGCTGCAGG TGGAGAGAAA CAGGAGGGGC GGCTGTGGTG AGCCGGGGCT GGCATCCACC 480
TCCTGGCGAC GCGACCTACC AGGGACCTTG CCAAGGGGCC TCAGTCAGCC TTCTGTTGAT 540
GACACGCTGA GGTCAGGACC AGGGCCACAG CCTGTGTCTG ACAAGAAGCA GTTTCCAGTT 600
ATTTGGTGAA TCAGTGCTGG GGGCCTGGCC TGAGGGGTCC AGGGAGTCAC ACCTGACTCC 660
ATGTCCCTCT TTCCCACAAA GTAGGAGAGC GCCATGGGTC ACCTGCCCGA AAAGGCAGGT 720
CCATCCTCTG CCTGCAGTCA GAACTCAGGG GGATCCCTGA GGCCGGCAGC AGAGCCACGA 780
GGACGCAGTG GCCTGGCGGC GGGTGGGGCA GCGCGGGAGC TGCTTTCCAG GCCAGACAGA 840
CGGAGCCGTT CTCCTGCCGG CCTTCCCGGG AGCAGGATCC CATCCAGTGA TGCGTAGGCC 900
TGTGGCGGGG ACAAGGAGGG CGGGCAGCTG CTTTTGTTTC CCATCTGCTT CTCTGGCTTG 960
GAAAGAAGGG CAGACAGCTC CAGAAATATC GAGGAACGTG GGCCACGCCT CCGGGGCGGC 1020
CACCAGGCGG TGGCACCAGA AGGTCAGCAG AGACAGAGCA TAAACAGCAG CCACACAAGA 1080
CACCCACGCG GGACACGGGC CGTGTGCGCA CATGGGCACC TGATGCCTGG TGGCCGAGAG 1140
GACAGCACGG CCTGAACACC CGGCAGGAGG GGACGGATGG TCCATCCACA CTGGAACATT 1200
ATCCCATGAC GAACCGGAGC CAGGCCACAG CGTGAACCTG GAGGACATCA TGCTCAGTCA 1260
CAGATGCCAA ACTCAGAAGG CCACGCAGTG TGTGATCCCA TTTCTATGAA CTGTCCGGGA 1320
CAGGCCCATC CAGAGACAGG GAGGGGATGT GTGGGTGTCG GGGAGTGACG GCTGATGGGG 1380
ACAAGGTTTG TTCTTCTCGA GGTGATAGAA TGCTGTAGAA TTGGAGGTGG TAGTTGCACA 1440
CTTTTCTGAA TGTACTACAT GCGACTGAAT TGTACACCTT AAATGAGTGA ATTGTATGGA 1500
ATGTGAATTA CAAATCAATG AAGATGCCCA GGCCGGGTGC GGTGGCTCAC GCCTGTAATC 1560
CCAGCACTTT GGGAGGCCAA GGTGGGCAGA TCACCTGAGG TCAGGAGTTC AAGACCAGCC 1620
TGGTCAACAT GGCGAAACCC AGTCTCTACT AAAAATACAG AAATTAGCTG GGTGGTGGCT 1680
TACGCCTGTA ATCCCAGCTA CTCAGGAGGG TGAGGCAGGA GAATCGCTTG AACCCAGGAG 1740
GCAGAAGTTG CAGTGAGCTG AGATGGCGCC ATTGCACTCC AGCCTGGGTG ACAGAGAGAG 1800
GCTCTGTCTC AAAAAGTAAG TAGGCCGGGC GTGGTGGTTC ACGCCTGTAA TCCCAGCACC 1860
TTGGGAGGCC AAGGGACGCA GAACACAAGG TCAGGAGTTC AAGACCAGCC TGGCCAAGAT 1920
AGTGAAACCC CGTCTCTACT 1940