EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-31246 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr8:145007520-145008160 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7003580chr8145007534hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr8:145008036-145008046GCCCCGCCCC+6.02
ZNF263MA0528.1chr8:145007859-145007880CCCTCCCCCAACCCCTCCCCT-6.3
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_09260chr8:145007117-145019257CD14
SE_10783chr8:145007280-145009796CD19_Primary
SE_11513chr8:145000243-145019270CD20
SE_12121chr8:145007152-145009402CD3
SE_14847chr8:145007671-145009319CD4_Memory_Primary_7pool
SE_16928chr8:145007367-145009831CD4p_CD225int_CD127p_Tmem
SE_17383chr8:145006613-145020039CD4p_CD25-_CD45RAp_Naive
SE_17884chr8:145006516-145019331CD4p_CD25-_CD45ROp_Memory
SE_18961chr8:145007374-145009580CD4p_CD25-_Il17-_PMAstim_Th
SE_19196chr8:145007074-145018699CD4p_CD25-_Il17p_PMAstim_Th17
SE_23034chr8:145007349-145009232CD8_primiary
SE_23089chr8:145007443-145021710Colon_Crypt_1
SE_23735chr8:145007456-145009146Colon_Crypt_2
SE_24704chr8:145005616-145021714Colon_Crypt_3
SE_26583chr8:145007009-145030049Esophagus
SE_28831chr8:145008081-145009000Fetal_Intestine_Large
SE_29600chr8:145007391-145009181Fetal_Muscle
SE_31395chr8:145007455-145021754Gastric
SE_34239chr8:145003594-145029511HCT-116
SE_34673chr8:145007097-145028424HeLa
SE_37176chr8:145007038-145028465HSMMtube
SE_38740chr8:145007497-145009278HUVEC
SE_40656chr8:145006888-145009318Left_Ventricle
SE_42376chr8:145006289-145021766Lung
SE_44278chr8:145007427-145009755NHDF-Ad
SE_44786chr8:145007430-145008249NHLF
SE_46680chr8:145008051-145008866Ovary
SE_47321chr8:145008032-145032287Panc1
SE_48066chr8:145006204-145021794Psoas_Muscle
SE_48646chr8:145006781-145009255Right_Atrium
SE_50057chr8:145007167-145021759Sigmoid_Colon
SE_51144chr8:145006191-145029766Skeletal_Muscle
SE_52367chr8:145008040-145009597Small_Intestine
SE_53601chr8:145006717-145021756Spleen
SE_54813chr8:145007192-145010076Stomach_Smooth_Muscle
SE_56139chr8:145007462-145009088u87
SE_56852chr8:145005920-145021728VACO_400
SE_61753chr8:145002108-145053930Toledo
SE_62528chr8:145001740-145054046Tonsil
SE_67795chr8:145007462-145009088u87
SE_68809chr8:145007569-145008772H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8145007800145007881
Enhancer Sequence
TGCAAGGTCG TTGCCATGAC TCGGAGCACA GCTGATCCCC CTCTGACCTC ACAGGGGCCC 60
CGGCCAAGAC GGCCACCCTC AGCCGCTTCC TCAGCCTCAG TGGGCCACTG CCTCCATCCC 120
TGTCCTTCCC CTTCCCTCCC TGCCCACCTC ACACATCTTC CTACTGGCCT TCTGGGGGAT 180
TGGGACCAAG TCCAGAGTAC TTAGCCCAGT CCAAGAACCG AGACCCCCAT GACCATGTCT 240
GTGGGGTCCT GGGCCTCATC CTCCATCACC CACCCTGGGT AACTCCTCCT GTAATGCCAC 300
GTGGGCCCTG TCCTCCTGGG CAATCAGCAG TGGGTTGGGC CCTCCCCCAA CCCCTCCCCT 360
AACAGTAAGC CGCTGTCGGG GAGGGGGCCT GGCGGGGGCA AGGCAGCCCA GCGTGGGTTC 420
TGCCCCGTGG CCAGAAACCA ACTCTGCCCA AAGCAGGCAG TGAGAGTTAG CTGCACACGA 480
GGAGGGAGGA GCTCAGGCCT GGATTCCCCA CCACATGCCC CGCCCCTGCC CCTGCCCCTG 540
CCCCAGGAGC CCAGGGGGAC AGCCCCCTCC TGGCTTTAGG GCTGCAGGGC GGGGCAGGCT 600
CCTCCGGCCT CCCTCCCGCC CACTGCCTGC CCCACACCCC 640