EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS042-30462 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr22:41839040-41840820 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF8MA0652.1chr22:41839651-41839665AGTTTCGGTTTTGT-6.1
IRF9MA0653.1chr22:41839651-41839666AGTTTCGGTTTTGTT-7.49
Number of super-enhancer constituents: 48             
IDCoordinateTissue/cell
SE_01131chr22:41839794-41844619Adrenal_Gland
SE_03173chr22:41839842-41842772Brain_Angular_Gyrus
SE_03911chr22:41839674-41845831Brain_Anterior_Caudate
SE_05807chr22:41837785-41845936Brain_Hippocampus_Middle
SE_06715chr22:41837746-41845767Brain_Hippocampus_Middle_150
SE_07758chr22:41837813-41839544Brain_Inferior_Temporal_Lobe
SE_07758chr22:41839582-41845809Brain_Inferior_Temporal_Lobe
SE_09106chr22:41839901-41840348Brain_Mid_Frontal_Lobe
SE_09106chr22:41840629-41842630Brain_Mid_Frontal_Lobe
SE_10820chr22:41839946-41845823CD19_Primary
SE_11307chr22:41837831-41839423CD20
SE_11307chr22:41839585-41845977CD20
SE_13251chr22:41839757-41844765CD34_Primary_RO01480
SE_17492chr22:41839594-41845604CD4p_CD25-_CD45RAp_Naive
SE_19674chr22:41839813-41845017CD4p_CD25-_Il17p_PMAstim_Th17
SE_23011chr22:41839757-41845435CD8_primiary
SE_23699chr22:41839861-41844674Colon_Crypt_1
SE_24304chr22:41839970-41844641Colon_Crypt_2
SE_25050chr22:41839843-41844693Colon_Crypt_3
SE_26976chr22:41838684-41839628Esophagus
SE_26976chr22:41839761-41845252Esophagus
SE_28149chr22:41839790-41845473Fetal_Intestine
SE_29275chr22:41839703-41845489Fetal_Intestine_Large
SE_29904chr22:41839609-41845852Fetal_Muscle
SE_31330chr22:41839814-41845749Fetal_Thymus
SE_31677chr22:41839771-41845326Gastric
SE_33048chr22:41840515-41844565H1
SE_35657chr22:41839802-41845500HepG2
SE_40631chr22:41838107-41839498Left_Ventricle
SE_40631chr22:41839580-41845358Left_Ventricle
SE_41678chr22:41839963-41844656LNCaP
SE_42535chr22:41839731-41845391Lung
SE_47777chr22:41839942-41840499Pancreas
SE_47777chr22:41840541-41844668Pancreas
SE_48064chr22:41837768-41845339Psoas_Muscle
SE_48879chr22:41838979-41845274Right_Atrium
SE_49646chr22:41839901-41844667Right_Ventricle
SE_50476chr22:41839752-41845486Sigmoid_Colon
SE_51256chr22:41838289-41845638Skeletal_Muscle
SE_52860chr22:41839749-41845359Small_Intestine
SE_53619chr22:41839724-41845350Spleen
SE_55020chr22:41839619-41845443Stomach_Smooth_Muscle
SE_55582chr22:41839854-41844824Thymus
SE_59590chr22:41839766-41845011Ly3
SE_60932chr22:41839770-41845402DHL6
SE_62805chr22:41839598-41845725Tonsil
SE_65292chr22:41838917-41845157Pancreatic_islets
SE_68868chr22:41839845-41844770H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr224183933241839605
Number: 2             
IDChromosomeStartEnd
GH22I041441chr224183788441839164
GH22I041443chr224183922141839605
Enhancer Sequence
TGAGAGCAAA ATTCTGTCCA ATTTCACTAA GAATTTTATC CTCACTTGTT TACTTCCAGC 60
AGCAAAGTTA AACCTGGATT CTGATCCCTT GTGCTGACTT GTGTTTTAAA GAGCAGGTGC 120
CTAGGAGAAA GACGACGGGG GAAGAAGTGG GGCGTGAAGC TCAAAAGAAG CCTCAGTCAG 180
TGCAGATTCC AGAGAGAACT TCTGATAAAA ATGTGAGGAA GGTGTGTGTG TGTGTCACAC 240
GCGCGCGCAT GTGTCTGCCT GCTCTAATGT CAGAAGCGAA GGAAGATTTT TTTCCCCCCC 300
TCGAGACAGT CTTGCTCTGT AGCCCAGAGC TGGAGTGCAA TGGCGCCATC TTGGCTCACT 360
GCAACCTCCG CCTCCTGGGT TCAACCAATT CTCCCGCCTC AGCCTCCCGA GTAGCTGGGA 420
TTATAGGCAC GCGGGACCAC GCCCGGCTAA TTTTTGTATT TTTAGTAGAG ACGGGGCTTC 480
ACCATGTTGG CCAGGCTGGT CTCGAAATCT TGACCTCGTG ATCCGCTCGC CTCCGCCTCC 540
CAAAGTGTTG GGATTACAGG CGTGAGTCAC TGCCTAGCCA GAAGATTTTT TTTTTTTTTT 600
TTTTGAGATG GAGTTTCGGT TTTGTTGCCC AGGCTGGAGT GCAATGGCGC GATCTCGGCT 660
CACCGCAACC TCCGCCTCCC AGGTTCAAGC GATTCTCCTG CCTCAGCCTC CCGAGTAACT 720
GGGATTACAG GAATGCGCCA CCACGCCCGG CTAATTTTGT ATTTTTAGCA GAGACGGGGT 780
TTCTCCAAGT TGGTCAGGCT AGTCTCGAAC TCCCGACCTC AGGTTATCCG CTGCCCGCCT 840
CAGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG CACCCGGCCG GAAGGTTTTT 900
CAGAAAGAAA ATTCTGTTTC AAAGAGGAAA AGGAGGGATA ATGGTGATGG AATCCACTGA 960
GCCCCAAACC CAAAAAGATA CTCAGACACC TCTAAGCCTT AAATGTGCAA ACTGTCCTAC 1020
AATGACGGAC TACAGGACTC AACTAAGTGT GGAGGGGCCA GCAGGTGTCA CAGACCGGGT 1080
GGATGCGAGT GCCCTGCCGC TGTCCGGGGA GTGAGAGCCA AACGCAGGCA GCTCCTCTCC 1140
TTGGTGAGAC ACGGGATCCG CCCCAACTCG CTGGTCCCAG AGGCAGCGGC CCAGACAGGC 1200
GGGTGTGTAT TGAAAGGCTT CCAGGACTGG TGCTGACTGA CTGCAACACC GCGCCCAGTC 1260
TCTCATCATC TCCCCCTAGA CACAGACCGG TCAACCTTAG GTCTGACAAC AAGGCCCCTT 1320
TCGGCTATGA AGACCCTTTC TAGGGCACTC CATGTTCCTC AGGAGCTAGG AAAACTCGAC 1380
TCAACCCAAA CGTAGGCGGA GAGGCGGGCG GTGAGGGCCC GCTCTGCACT CTGGGAATTG 1440
TAGTCCTCAA ACACCTCCGG ACCAGGCGAT AGCAGGAGTG ACCTACTTTC CCTGCACACT 1500
ACACTTCCCT GAGCACTTTG CGAAGGCCCA ACTGGCCGCA ATACGCATGC CCGGTAAGGG 1560
GAGCCGACCG AGGGTCGAAG AGCCCAGGAA AAGTTTCCGA TGCACATGCG CGCTGAGGCG 1620
GGTCGGCGCC CCCCTCCCAT CGCCTAATAC ATTTCATGTA GATTCTACCC AAAAGGCCTA 1680
CTCCCCGTAT TGTATGGCCC CACCACATCC TCTAGGCTTT ACGAGAGCCT AACTTTCCCA 1740
CCTTTCCCTT CATCGCCTCC CATTACTGAT GAAACTAGGA 1780