EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS003-02151 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr1:145455000-145456220 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:145455546-145455564CCTTCCTCCCCACCCTCC-6.05
IRF1MA0050.2chr1:145455653-145455674GAACCAAAAGAGAAACTGCAA-6.35
NFYAMA0060.3chr1:145455452-145455463AGCCAATCAGA+6.32
RORAMA0071.1chr1:145455882-145455892ATCAAGGTCA+6.02
Spz1MA0111.1chr1:145456138-145456149GCTGTAACCCT-6.14
ZNF263MA0528.1chr1:145455546-145455567CCTTCCTCCCCACCCTCCTTA-7.32
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_00756chr1:145445696-145457979Adipose_Nuclei
SE_01458chr1:145453947-145456607Adrenal_Gland
SE_02981chr1:145454040-145455411Bladder
SE_02981chr1:145455546-145457319Bladder
SE_03588chr1:145454655-145457763Brain_Angular_Gyrus
SE_09909chr1:145452833-145457759CD14
SE_10440chr1:145451159-145457893CD19_Primary
SE_11279chr1:145447991-145458401CD20
SE_12082chr1:145453935-145457759CD3
SE_13107chr1:145454104-145456911CD34_Primary_RO01480
SE_13542chr1:145453953-145458029CD34_Primary_RO01536
SE_15429chr1:145453903-145457805CD4_Memory_Primary_8pool
SE_15878chr1:145454078-145457565CD4_Naive_Primary_7pool
SE_16566chr1:145454108-145456556CD4_Naive_Primary_8pool
SE_17274chr1:145453904-145457907CD4p_CD225int_CD127p_Tmem
SE_20184chr1:145452124-145457976CD56
SE_20813chr1:145453796-145457821CD8_Memory_7pool
SE_21574chr1:145453862-145457891CD8_Naive_7pool
SE_22030chr1:145453826-145457897CD8_Naive_8pool
SE_23056chr1:145451132-145458039CD8_primiary
SE_23523chr1:145453975-145457413Colon_Crypt_1
SE_24422chr1:145454745-145456490Colon_Crypt_2
SE_25816chr1:145450728-145458036Duodenum_Smooth_Muscle
SE_27997chr1:145453945-145457665Fetal_Intestine
SE_29253chr1:145453872-145457664Fetal_Intestine_Large
SE_29607chr1:145450648-145457590Fetal_Muscle
SE_31291chr1:145453921-145457546Fetal_Thymus
SE_31806chr1:145451235-145457833Gastric
SE_34844chr1:145453683-145458024HeLa
SE_37342chr1:145447588-145458514HSMMtube
SE_40272chr1:145453716-145457723K562
SE_41151chr1:145447968-145458010Left_Ventricle
SE_42752chr1:145448015-145457936Lung
SE_43539chr1:145447700-145458154MM1S
SE_49674chr1:145454712-145455274Right_Ventricle
SE_49674chr1:145455595-145456357Right_Ventricle
SE_50886chr1:145451288-145458138Sigmoid_Colon
SE_51429chr1:145445775-145457866Skeletal_Muscle
SE_52426chr1:145453947-145458135Small_Intestine
SE_53983chr1:145451316-145458238Spleen
SE_55165chr1:145454015-145457661Thymus
SE_62640chr1:145448375-145458373Tonsil
SE_67213chr1:145447700-145458154MM1S
SE_67763chr1:145453987-145457805u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1145455122145455741
Number: 1             
IDChromosomeStartEnd
GH01I145976chr1145447474145458120
Enhancer Sequence
TTTGTTGCCT AGACTGGTCT CAAACTCCTG GCTTCAAGCA ATCCTCTTGC CTCAGTCTTC 60
CAAACTTCTG GGATTACAGG CTTGAGCCAT GGCACCTGCC ATTGCTTCTA TGTAAACACT 120
AACTAACACA CCCAAACTAG GCTTTTAAGG TGCTTTCCCT CAATGGAGTC ACAGTCTTTC 180
TTCATTCTTT ACAATGGGGT CAGACATATT CAACCTTAGA TTGACAGTCT CTATCACTTG 240
ATGCTGTAGG GAATTCAGTC GGCCTGCCTG AATGCAGTTG GGGAATTTTT TGAAGGTTCT 300
TCTATACCCC ATCTTACGGC TTTCAAATGC TCAGCAGGGT TGCTATGATA GCATGCCTTC 360
TTATTCAGTT CCTATTCTGG ACACGCAGCT TGCCCGTGAC TGTTGCATGT CAAGTGGCTG 420
GAACCAATCA GCTTATCTAA GGCTTCCTCA GAAGCCAATC AGAGCCTCGG AAAGTGACCT 480
CACCCAAGGG AGAGCTCTGT GGGCGAGAAA GCATCTCTCA GATCTGTGAG TGTCCCTAAG 540
TCACTCCCTT CCTCCCCACC CTCCTTACTT CCTGTAAAAC AACACCACAC CGCCTACCTC 600
CCTTCCCCCA AAGAAAGGGA GTGAGAAAGG CTAACTAAAT TCCACAAAGG GAAGAACCAA 660
AAGAGAAACT GCAACTCAGC CACACACTGG TTTCTGTAAC TGGAGAACAG GATATTTAGG 720
GGGACTTGCT CTGCACAGAC ATACCTTTCA AAGTGGCATC TCCAGAGTCT GGAAGAGGAG 780
GGAGTATGGT GAATAAGTCA GCTCCTCCTC CCTCCTCATA CCTGGTTTTC TTGCCTTTCC 840
CCACAAAAAT AGCTGTAATC ATTTTTTGTA AATAAGGACA AGATCAAGGT CAAGTGTGGG 900
AAAGACAGGA CCTATGTCCT TGTGAACATG TGTGAACAGA CACAATCATG TCCTTGTGGC 960
CTGAGGACCA GAGGCTCAGA AGTCAGCTGT ACTGCAGGGG GCGTAGGCTG TTCTCTACAA 1020
TTTACTTTGC ATTGCCCTAC AGATGAGGCC TTGAATATTC CTTGGCTGGG CTCGATTGTG 1080
AATATGTGTC CCACCATGGG GGTAGAAGGG AAGGGACAAA GGACAAGCGG GCTGTAGGGC 1140
TGTAACCCTC CAGTGTGTCA CACCAGACCC GGCTTAGTTA AGCATTTCCT TCATTCCTCC 1200
AGCCCTCTGT CACCAGGCCT 1220