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

TagContent
EnhancerAtlas ID
HS105-26116 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr14:105531040-105531710 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE41MA0636.1chr14:105531207-105531217GTCACGTGAC+6.02
BHLHE41MA0636.1chr14:105531207-105531217GTCACGTGAC-6.02
HNF4GMA0484.1chr14:105531367-105531382CAGGGACAAAGTCCA+6.19
Hnf4aMA0114.3chr14:105531368-105531384AGGGACAAAGTCCAGC+6.62
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_09608chr14:105524305-105534530CD14
SE_10756chr14:105529270-105534705CD19_Primary
SE_11338chr14:105524210-105537963CD20
SE_12224chr14:105530306-105534527CD3
SE_16243chr14:105530881-105534696CD4_Naive_Primary_7pool
SE_16755chr14:105529355-105534256CD4_Naive_Primary_8pool
SE_17159chr14:105530332-105534429CD4p_CD225int_CD127p_Tmem
SE_17455chr14:105524129-105534755CD4p_CD25-_CD45RAp_Naive
SE_18037chr14:105524469-105534677CD4p_CD25-_CD45ROp_Memory
SE_19270chr14:105524758-105534459CD4p_CD25-_Il17p_PMAstim_Th17
SE_20593chr14:105530316-105534450CD56
SE_21861chr14:105530504-105534625CD8_Naive_7pool
SE_22228chr14:105530041-105534539CD8_Naive_8pool
SE_22674chr14:105524525-105534718CD8_primiary
SE_59559chr14:105527286-105560991Ly3
SE_62889chr14:105524889-105561202Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14105531089105531459
Enhancer Sequence
TTGTGCTCAG CCCAACTGGC CAGTCTTCAG TGGTCAGTCC CAGTCCCTTG CAGTGGTACA 60
GACCCACGTC ATGCACTTGA CAGAAGGTAT TGGGCCCCCC GCCCCGCTGT GCCTGGTGCG 120
CCGAACGCCA CTCCAAAGGC CGGTGACCTG CCCAGCTCCA GGATCTTGTC ACGTGACTGG 180
GCCAACTGCC ACTCACCGCA GCACAGCCCC CACTGCCCTG CTTTTCCCTC TGTGTAACCC 240
CACAAGCAGC ACAGGCCCCA CAGAGAGAAG CCCAGCCCTT CAGTGCCCCC CGACCAATCA 300
CGGAAGCAAG TGGCCAAGGA GAGATTCCAG GGACAAAGTC CAGCCCCCTG ACTCACCCCC 360
ATCTGGACCA GTAGCCAGGG AAGCCTTTTC CAGAAGAAAG TCTCCAGGAA GGTGGCGGTG 420
ACAAAGATAC AATGGAAACT GTTGTCCCTC TCCCCCAAAT CCTCCGGCCC CATCACATCT 480
GTGGTCACTG GGGGTCCTGG GTTCTCTCGG GAGGGACCCC AGATTAAGAA CCCTCAACAA 540
AGCCTCCATC TTTACCAACA AATCACCTTT GCCTTCAGAT CCCCCTCTGC CCGCCTCCAG 600
CTCCCAGCCC CCAGCCCCAT CCCAGAGCCT GGCCCCCCAG GCCCACTCCC CAGCACGCAG 660
AGCCCAGCGA 670