EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-13985 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:18404840-18405980 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4808779chr1918404936hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr19:18405221-18405232CCACACCCTCT+6.02
MAFFMA0495.3chr19:18405572-18405587ATGCTGACTCAGCGG-7.13
MAFFMA0495.3chr19:18405572-18405587ATGCTGACTCAGCGG+7.18
MAFKMA0496.2chr19:18405570-18405589TGATGCTGACTCAGCGGCA-6.04
RREB1MA0073.1chr19:18405040-18405060GGGTGGGGGGTGGCTTGAGT-6.06
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_02921chr19:18404746-18405622Bladder
SE_05533chr19:18401730-18405557Brain_Cingulate_Gyrus
SE_08373chr19:18400681-18406547Brain_Inferior_Temporal_Lobe
SE_08865chr19:18404921-18405068Brain_Mid_Frontal_Lobe
SE_08865chr19:18405079-18405418Brain_Mid_Frontal_Lobe
SE_10202chr19:18404819-18405777CD19_Primary
SE_11066chr19:18399930-18406669CD20
SE_11848chr19:18400446-18406390CD3
SE_15471chr19:18400430-18406563CD4_Memory_Primary_8pool
SE_15863chr19:18401810-18406353CD4_Naive_Primary_7pool
SE_16357chr19:18400587-18406381CD4_Naive_Primary_8pool
SE_16887chr19:18400579-18406453CD4p_CD225int_CD127p_Tmem
SE_19999chr19:18400047-18406146CD56
SE_21483chr19:18400639-18406680CD8_Naive_7pool
SE_22027chr19:18404603-18406485CD8_Naive_8pool
SE_22337chr19:18400391-18406271CD8_primiary
SE_24690chr19:18404952-18405823Colon_Crypt_3
SE_34794chr19:18401766-18405666HeLa
SE_43324chr19:18401834-18406232Lung
SE_54453chr19:18400417-18405596Spleen
SE_54691chr19:18400553-18405181Stomach_Smooth_Muscle
SE_55149chr19:18405082-18405481Thymus
SE_59111chr19:18389483-18418456Ly3
SE_61379chr19:18395257-18419023HBL1
SE_61915chr19:18389769-18420206Toledo
SE_68630chr19:18390487-18416372TC71
SE_68631chr19:18390487-18416372TC71
SE_68632chr19:18390487-18416372TC71
SE_68759chr19:18401859-18405645H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191840532618405850
Number: 1             
IDChromosomeStartEnd
GH19I018289chr191839997718406115
Enhancer Sequence
TCACCATATT GGCCAGGATG GTCTCCACCT CTTGATCTCG TGATTCGTCC GCCTCAGCCT 60
CCTAAAGTGT TGGGATTACA GGCGTAAGCC ACTGTACCCG GGCTGAATTT GAGGTGTGTT 120
AAGGGAACAT CCAGGAGGAG GCGTGGCGCA GGGTGAGGAG AGATGGAGGA TTACAGGGGC 180
CTCCAGATCC TAAGCAGGGA GGGTGGGGGG TGGCTTGAGT CCTTGGCCAG CCCAGGTGGA 240
GCCTGTGACT GCTCTCCCTG CCTCACTTTT CCTACCATTA TGCATGCTCC AGAAGCAGCA 300
GGGGAGGCTT TGGGGATGTG GAGGTTGCCC AGGGTCACAG GGACCCCTGT TGTGCCCTCC 360
GTCAGTGCCC CTCTGGCCTC CCCACACCCT CTGTGGCTCC CTGCTGTGGC CAGTCTTCCC 420
CATCATCGCC CCTGGCTCTC TTCTCTCCTG CAGTCCAGCC ACTCAGCCCT TGTACATGTC 480
CCTCATCTGT TCTCACAATG CCCACCCCAG GTGACAACAT CCTCCCAAGC CCCCTTCAGG 540
AGATGGTGGG GCTGACACTA ACAGGGGAGG GGGTGTAGGG AAGGTGAGCA CCCTGGCCCC 600
TGAGTGCTGC ACACAAACTG TGTAAAAATA GCTGCTCCCC CTGCCCCCTG TGAGGAGGCG 660
GCTGTGACGG TGGTGGCTGC AGTGACGGGG ATGTGCCCAG AGAAGCATCC GGCAGGGCCA 720
GTTGCCATGG TGATGCTGAC TCAGCGGCAG AGGCAGGTAG CAGCATCTGG TACCCGGCCG 780
GCACGCCTCT GCTTGGCCTA CGCTCATAGC ACCCTGTCCA GCCCCAACTT TCCAGCCTCC 840
ACCCTGGGGG TGTCTTCTGA GGCTGCAGAG GGGTGGGTGA GACCTCGGGA AGGACTGGAC 900
AAGTTCCTCC ACCAGACACC ACTCAGTCAT CTGCTGGAAG GTGGGAGACG CTGCTTCTCA 960
TGGAGCGGAC CTCAGTGTCA GGTCTTCCTC CCTCTATCAG CCATCCGCCC ATCTACCTAC 1020
TCACCCATCC ATCCACTCAT CCACCATCCA CTCATCCCCC ATCCATCCAC CATCCACCCA 1080
TCCATCTACC ATCTGCCCAT CTACCATCCA TCCACCCACC TGTCCATCTA TCCACCCATC 1140