EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS139-27230 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr19:49379320-49380440 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr19:49379886-49379907AACAGGAAAGTGAAACAGGAG-6.54
PAX5MA0014.3chr19:49379904-49379916GAGCGTGACCGC+6.07
SOX10MA0442.2chr19:49379394-49379405AAAACAAAGCA+6.02
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_02582chr19:49375353-49379744Astrocytes
SE_09874chr19:49375167-49380182CD14
SE_10451chr19:49375264-49380143CD19_Primary
SE_11592chr19:49375087-49380263CD20
SE_12031chr19:49375357-49379805CD3
SE_12911chr19:49375389-49379802CD34_Primary_RO01480
SE_13446chr19:49375209-49380162CD34_Primary_RO01536
SE_14160chr19:49375148-49379802CD34_Primary_RO01549
SE_14516chr19:49374907-49380097CD4_Memory_Primary_7pool
SE_16006chr19:49377835-49379480CD4_Naive_Primary_7pool
SE_16449chr19:49375053-49379829CD4_Naive_Primary_8pool
SE_17011chr19:49375172-49379796CD4p_CD225int_CD127p_Tmem
SE_18005chr19:49375034-49380135CD4p_CD25-_CD45ROp_Memory
SE_18664chr19:49375002-49380492CD4p_CD25-_Il17-_PMAstim_Th
SE_19244chr19:49375001-49380219CD4p_CD25-_Il17p_PMAstim_Th17
SE_20386chr19:49375217-49380086CD56
SE_20818chr19:49375164-49380071CD8_Memory_7pool
SE_21614chr19:49375342-49379568CD8_Naive_7pool
SE_22825chr19:49375139-49380025CD8_primiary
SE_23444chr19:49378407-49379634Colon_Crypt_1
SE_25067chr19:49378392-49379557Colon_Crypt_3
SE_26423chr19:49375143-49380219Duodenum_Smooth_Muscle
SE_27511chr19:49374808-49380043Esophagus
SE_28037chr19:49375002-49379938Fetal_Intestine
SE_29055chr19:49374886-49379972Fetal_Intestine_Large
SE_29864chr19:49374926-49379804Fetal_Muscle
SE_32151chr19:49374786-49380087Gastric
SE_34926chr19:49374664-49380013HeLa
SE_36532chr19:49375182-49379790HMEC
SE_37651chr19:49375001-49380114HSMMtube
SE_38685chr19:49375133-49380223HUVEC
SE_40239chr19:49375236-49379941K562
SE_41238chr19:49375070-49379930Left_Ventricle
SE_42580chr19:49374908-49380132Lung
SE_44613chr19:49375250-49379775NHDF-Ad
SE_44996chr19:49375073-49379829NHLF
SE_49212chr19:49375375-49379804Right_Atrium
SE_50975chr19:49375052-49379810Sigmoid_Colon
SE_51362chr19:49374930-49380063Skeletal_Muscle
SE_52923chr19:49375123-49380113Small_Intestine
SE_53855chr19:49374962-49380180Spleen
SE_59232chr19:49361792-49396070Ly3
SE_64565chr19:49375203-49379863NHEK
SE_65554chr19:49374686-49379805Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr194937956549380240
chr194938035149380412
Enhancer Sequence
CAGCGTCTGT ATGTGTCAGA AACTGACAGC ATTCTACTTA CAGGTCCCTG AGGGAGCTGG 60
GAAGAGAATA GCATAAAACA AAGCACTTCA ATGGCGGATA AACCGCTTTT CCTCAAATTT 120
GCTACCACTC ATCCTGAGGC TTCTTTTGAA CCTAACAGTG CAGGGACCAG CCCCACAGGG 180
TCGGTGGGCT TCTCCCTGTG TGCGGCGACG AGAGAGTGTA GAAATAAAGA TACAAGACAA 240
AGAGATAAAA GAAAAGACAG CTGGGCCCGG GGGATTACTA CCACCAATGC GCGGAGACCA 300
GTAGTGGCCC CGAATGTCTG GCTGCGCTGA TATTTACTGG ATACAAAGCA AAAGGGGCAG 360
GGTAAGGAGT GTGAGTCATC TCCAATGATT GATAAGGTCA CACGAGTCAC GTTTCCACCG 420
GACAGGGGGC CCCTCCCTGT TTGGCAGCCC AGGTGGAGAG AGAGAGGAGA CAGCTTATGC 480
CATTATTTCT GCATTTCAGA GACTTTTAGT ACTTTTACTG ATTTTGCTAC TGCTATCTAG 540
AGGGCAGAGC CAGGTGCACA GAGTGGAACA GGAAAGTGAA ACAGGAGCGT GACCGCTGAA 600
GCACAGCATC ACAGGGAGCC GGTTAGGCCT CCGGATAACT GTGGGCCAGC TTGACTAATG 660
TCAGGCCCTC CACAAGAGGT AGAGGAGCAG AGTCTTCTCT AAACTCCCGC AGGGAAAGGG 720
AGACTCCCTT TCCTGGTCCG CTAAGTAGCG GGTGTTTTTC CTTGACACTG AGGCTACCGC 780
TAGACCATGG TCCACTTGGC AACGGGCGTC TTCCCAGATG CTGGCGTTAC CGCTAGACCA 840
AGGAGCCCTT CTGCTGGCCC TGTCCGGGCA TAACAGAAGC CTCGCACTCT TGTCTTGTGG 900
TCACTTCTCA CTATGTCTCC TCAGCTCCTA TCTCTGTATG GCCTGGTTTT TCCTAGGTTA 960
TGATTATAGA GCGAGGATTA TTATAATATT GGGATAAAGA GTAATTGCTA CAAACTAATG 1020
ATTAATGATA TTCATATATA ATCATATCTA AGATCTATAT CTGGTATAAT TATTCTTGTT 1080
TTATATTTTA TTATACTGGA ACAGCTCATG TCCTCGGTCT 1120