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

TagContent
EnhancerAtlas ID
HS017-00599 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr1:27889860-27892190 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr1:27890271-27890282GCTTCCCGCCC-6.02
HNF4GMA0484.1chr1:27890632-27890647GGAGGCCAAAGTCCA+7.22
Hnf4aMA0114.3chr1:27890633-27890649GAGGCCAAAGTCCAGG+6.26
RREB1MA0073.1chr1:27891686-27891706CCCCCACCCACCCGCCGAGG+6.28
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00527chr1:27889462-27891915Adipose_Nuclei
SE_00861chr1:27886075-27904718Adrenal_Gland
SE_01588chr1:27886149-27904879Aorta
SE_02913chr1:27890049-27890615Bladder
SE_02913chr1:27891079-27891732Bladder
SE_03261chr1:27889156-27892628Brain_Angular_Gyrus
SE_03939chr1:27886198-27895237Brain_Anterior_Caudate
SE_05478chr1:27885928-27895152Brain_Cingulate_Gyrus
SE_05814chr1:27880294-27902223Brain_Hippocampus_Middle
SE_06945chr1:27886514-27895216Brain_Hippocampus_Middle_150
SE_07770chr1:27885748-27895172Brain_Inferior_Temporal_Lobe
SE_08953chr1:27890875-27891588Brain_Mid_Frontal_Lobe
SE_14757chr1:27885672-27892439CD4_Memory_Primary_7pool
SE_23479chr1:27888886-27895065Colon_Crypt_1
SE_24168chr1:27889383-27892160Colon_Crypt_2
SE_24711chr1:27889725-27892508Colon_Crypt_3
SE_25901chr1:27889480-27892932Duodenum_Smooth_Muscle
SE_26518chr1:27885702-27904919Esophagus
SE_27625chr1:27889852-27891463Fetal_Intestine
SE_28547chr1:27889632-27891469Fetal_Intestine_Large
SE_29557chr1:27886726-27904956Fetal_Muscle
SE_31394chr1:27886081-27904513Gastric
SE_33503chr1:27886818-27904912H2171
SE_34367chr1:27889551-27891748HCT-116
SE_34755chr1:27889435-27891507HeLa
SE_36974chr1:27887536-27905229HSMMtube
SE_39896chr1:27887871-27891386K562
SE_40593chr1:27885841-27904966Left_Ventricle
SE_42106chr1:27886079-27904957Lung
SE_46630chr1:27886679-27892191Ovary
SE_47670chr1:27888826-27892075Pancreas
SE_48058chr1:27885887-27904727Psoas_Muscle
SE_48567chr1:27886102-27904727Right_Atrium
SE_49444chr1:27886820-27892209Right_Ventricle
SE_50130chr1:27886169-27892585Sigmoid_Colon
SE_51091chr1:27886184-27904991Skeletal_Muscle
SE_52467chr1:27889204-27891715Small_Intestine
SE_53892chr1:27886040-27904947Spleen
SE_54527chr1:27885939-27904929Stomach_Smooth_Muscle
SE_65253chr1:27886204-27900313Pancreatic_islets
SE_68682chr1:27886365-27891995H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12788986027891017
Number: 1             
IDChromosomeStartEnd
GH01I027559chr12788613127905256
Enhancer Sequence
CACACACACA CACACACACG TGGGACAAGT CCCATCTTCC AGGTGTGAGG AAGGCATGGA 60
CCCCTCCACC CACCACACAG CATGAGGCAG GGACATAACC TCGCCCCTGC CTGGGAATCC 120
TCCCTGCAGA CTGTGGGATG GGTACACAAC ATGTCACCTC CCCGGCTGCC TTGGACAGGT 180
GACAGCCCAC CTCACCCCTC CCCCATCACT GTCACCAGCC TGGGTGGTGC CGTCCCTCTG 240
CCTGCAGAGG CGTCACAGCT CACACGGCAT GAATGTCACC CCAGCACTGC CAGAGCCGGG 300
CACAGCCACA CATTGCCCCA GTGACAAACA CCACTGGCCC CAGAGGAGGT GAAGGCACAC 360
AGGGCTCTGG TGTGACCTTG GCCTCTGGAC ACCAGGAGGG GAGGTGCTGT GGCTTCCCGC 420
CCAGTGGCGG GTGCTGGGGG AGAGGAGTGC TGGGGAGGAA GCTGCCTGGA CACACTGACT 480
ACCTGGAAAT GCCACCTCCC CCAGCCCTCA CTCCACTCCA TTTCTTATTC ACTGTAGTTG 540
TGTATCTAGG GAGGGGGCTG AATGAGTGGT GGAGGGAGGG CTGTCCTGAG GCGCTGTTAC 600
TATGAGACTG CTTAGAGATC AGTGGGGAGT AGGGCGGTTA GGGGTTGCTA TCACCATGTG 660
CTCAGTGGGA AGAGTATGGG ATAATGGCTT GAGACCCCCA TAGCTTCCAG GGGAGCCCTT 720
CTTCCTTACA AAGGCCCCCT CTCCAAACTT CAGGCCACAG AGCTGGGGAC AAGGAGGCCA 780
AAGTCCAGGA ACATGACTCA CCCAGGGAAC AGGCCCAGCC TGCTGGCCAT AGTGGTGAGG 840
GAGGCCAAGA GCCAAGAGGC CTGGGTTCCA GTCTGAGCTC CTCCAGGGCC AAGCTGGGTG 900
ACCTTGGAGC AGCAGCTCAG CCTCTTTGGC TTCGGGGAGG GGGGAAGGGG CCGCAGTGAG 960
AGAAGTGCCA GGGTCAGAAA GAAGAAGCTG AAGCTGGAGA CCAGCAGGCA GAACTTCAGG 1020
CCACAGAGGG CTCCAGCCCG CCTCCCCTGC TCCCCTGCTT CCTCACAAGG AACCTCATCT 1080
TCCTCATCTG TACAAAAGGG ACAAGAGTGC CAGCCTCATG AGACAAGGTA GCATAAAGTG 1140
GGCCGCTCCT CAAGAAATGG GAAGCTTCTG ATTGAAGAGA GGGAGAAATA GACTAAGAGA 1200
CTTGCCCAAG CCACAGAGCA AATTAGGATC AGCTGAACTC AGCCTCCATC TCCTGGCTCC 1260
CCACCTGGAG CTGTTTCTTT AAGACTGCTT GGAGGTCAAG TGTGGAGGGG GACAGGGGAG 1320
ATGTTGGGGT GTTGTTGGAT GCAGTGCCTC CCTGCCGCCC GATGAAGACC AATGAATCTG 1380
ATAGGAGTCC ACCATGCCCT ACCTTTACCC TAAACCCCAC TTGGCCCAAA GCTTGGACAA 1440
GAGGAGTGGC TCTAAGGGGA GGGAGGCACC CCACCTCCCA CCCCATCATG ACCAGCAGCA 1500
GCACCTGGTG CTTGGAAGGA CTAGAGGACC TGAGATGTCA GTGTCTAGGG CCCCTCGTTT 1560
TACAGGAGCC CAGAGAGGGA AAGGCCTAGC CTGAGGTCAC ACAGCACGAC AGCACAAGAG 1620
CCTAGAGTCC TGGCCACGGA CAGCCTCAGA GCAGAGTCCC CCTAGCCCCT GGGGGTGGCT 1680
GGAGCTGGGG GGCCCTGGGG GACTGAGTAA AGCGTGGCGA CAGATGGCCT GCCGAGGCAG 1740
CGGCGATCTG GGCGGCTGGC AGGCATGCTC GCTCCCGCGC AGGGAAGCGG CTAATTTTAG 1800
CTGAGGCCTC GATGCCAGCT TTGTTCCCCC CACCCACCCG CCGAGGGGGC CCAGCATGCC 1860
TTGCGTGCAA CCTGCCTCCC CCAGGCACCC CTACTCCCCC GCCTGGCCCC TTGGTGAGTA 1920
GTGCCCAGAC CCCAGGATCC TAGAACGGTC TGCCTGACCA GGCCTCACCA CACCCAGAGG 1980
TGAGGCCTGA CTCCCCTACC CCAGGGCCTG TTTGCCCACG ACTCCAAGCT CATTCCATGA 2040
AGAGGGGCGA GAGAGGAAGG ACAGAGGCCA CTGCCCAGAC TGGGAGGGCG GGCCAGACAG 2100
CAGGGGCTGC CAGTCTTGAA GGGAGGCGAG GCACTGTCCT CCACCCAACC CTTAAGGAGA 2160
CAGGACCCTG ATTCCACCCA TGCCCTGGAC AAACATTCTG TCTGGTGTCC CCCGGCGCTG 2220
GTGAGCAAGG GGCGGGAGTC ACTCTAGTCT TTCCTTGTTC CTCATAACTT TGAGTTTGTT 2280
CCAGGAACTC AAAGCACTTT AAAGAAGTCA GACATGAAGC AAGGATAGTA 2330