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

TagContent
EnhancerAtlas ID
HS116-16722 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr19:4049240-4050100 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RESTMA0138.2chr19:4049477-4049498GGCCCTGTTCCAGGTGCTGAA-7.29
Number of super-enhancer constituents: 17             
IDCoordinateTissue/cell
SE_00556chr19:4049923-4053993Adipose_Nuclei
SE_04973chr19:4049183-4050152Brain_Cingulate_Gyrus
SE_05886chr19:4049142-4054407Brain_Hippocampus_Middle
SE_09464chr19:4049379-4054371CD14
SE_23073chr19:4049204-4050148Colon_Crypt_1
SE_23728chr19:4049235-4050129Colon_Crypt_2
SE_24683chr19:4049267-4050091Colon_Crypt_3
SE_26575chr19:4049218-4050143Esophagus
SE_27700chr19:4049198-4049962Fetal_Intestine
SE_31428chr19:4048766-4050860Gastric
SE_41127chr19:4049212-4050107Left_Ventricle
SE_41816chr19:4049290-4049701LNCaP
SE_47637chr19:4049412-4049601Pancreas
SE_48492chr19:4049012-4050852Psoas_Muscle
SE_48938chr19:4049217-4050193Right_Atrium
SE_50061chr19:4049238-4050100Sigmoid_Colon
SE_65287chr19:4048846-4053724Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1940493104050005
Number: 1             
IDChromosomeStartEnd
GH19I004049chr1940492274054233
Enhancer Sequence
CCCAGGCTAA TCTCAAACTC CTGGGCTCAA GTGATCCTCT TGCCTCGGCC TCTCAAAGCT 60
CTAGGATTAC AGGTGTGAGC CACTGCGCCC GCCATGAACC CCTTTCCCTA CCACAGAAGG 120
AGACAGTGGG CTTCTGCCAC TCCATCCTGC CCCTACCCCT GGGGTAGGAT GAGGCCAGCC 180
AGTGCCTGGT GCCTTCATTC ATGCCACAGA CCTTTGCCGA GCGCCCGCTG AGGGCCAGGC 240
CCTGTTCCAG GTGCTGAAAA TACCGCAAGG AACAAGACAG GCAAACATCC CTGCCCTCTC 300
GAGGCTGGCG GCGGCCGAGG TGTTTGGTGA CAGATAGGGT GACCAACTGT TCTGGTTTTA 360
GCACTGAAAG TCCTGCATCC TGGGAAACCC CTCTGTCCGG GACAAAGTGG GGCAGTTGGT 420
CACCCTAGTA ACCAAGTCCC CACCCCACGA CACCCAGGAC TGCCCACTCT CCCCTCACTT 480
CAGCGTCACT CCCCTATCTG GGCTCCACCC TGACGTGCAA AGGTGCAAAG CACAAGCTAC 540
GCTGGGGCCT TTGCATGTGC TGCTCCCGCA GTCCGGGGTA CTTTCTTTTT TCCTCCTGGA 600
TCTTCACAGT CAAATTTGGG CTCAAATGTC ACCTCCTTCC CCAGCCCTGT CTCCATCCTC 660
CTGTCATCAC CACCTGACTC TTCTATTGTT TTTTTTTCTG AGACCGAGTC TCGCTCTATC 720
TTCCAGGCTT GAGCGCAGTG GTGTGGTCTC CGCTCACTGC AACTTCCGTC TCCCGGGTTC 780
AAGCAATTCT TCTGCCTCAG CCTCCCAAGT AGCTGGGATT ACAGGCCCTC TGCCACCACA 840
CCTGGCTCAT TTTTGTATTT 860