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

TagContent
EnhancerAtlas ID
HS102-00545 
Organism
Homo sapiens 
Tissue/cell
HuCCT1 
Coordinate
chr1:27889690-27891800 
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: 3             
ChromosomeStartEnd
chr12788986027891017
chr12788972427889774
chr12788980027891375
Number: 1             
IDChromosomeStartEnd
GH01I027559chr12788613127905256
Enhancer Sequence
AGACACACAC ACATGCACAC ACACACAGAA CCTGTCACAC AGCTGACCAA GACACACACA 60
CACGCACGCA TGCATGCACA CACCCACACA AAGAACCTGT CACATAGTTG ACCAAGACAC 120
ACACACATGC ACACACACAC AGAACCTGTC ACACAGCTGA CCAAGACACA CACACACACA 180
CACACACACG TGGGACAAGT CCCATCTTCC AGGTGTGAGG AAGGCATGGA CCCCTCCACC 240
CACCACACAG CATGAGGCAG GGACATAACC TCGCCCCTGC CTGGGAATCC TCCCTGCAGA 300
CTGTGGGATG GGTACACAAC ATGTCACCTC CCCGGCTGCC TTGGACAGGT GACAGCCCAC 360
CTCACCCCTC CCCCATCACT GTCACCAGCC TGGGTGGTGC CGTCCCTCTG CCTGCAGAGG 420
CGTCACAGCT CACACGGCAT GAATGTCACC CCAGCACTGC CAGAGCCGGG CACAGCCACA 480
CATTGCCCCA GTGACAAACA CCACTGGCCC CAGAGGAGGT GAAGGCACAC AGGGCTCTGG 540
TGTGACCTTG GCCTCTGGAC ACCAGGAGGG GAGGTGCTGT GGCTTCCCGC CCAGTGGCGG 600
GTGCTGGGGG AGAGGAGTGC TGGGGAGGAA GCTGCCTGGA CACACTGACT ACCTGGAAAT 660
GCCACCTCCC CCAGCCCTCA CTCCACTCCA TTTCTTATTC ACTGTAGTTG TGTATCTAGG 720
GAGGGGGCTG AATGAGTGGT GGAGGGAGGG CTGTCCTGAG GCGCTGTTAC TATGAGACTG 780
CTTAGAGATC AGTGGGGAGT AGGGCGGTTA GGGGTTGCTA TCACCATGTG CTCAGTGGGA 840
AGAGTATGGG ATAATGGCTT GAGACCCCCA TAGCTTCCAG GGGAGCCCTT CTTCCTTACA 900
AAGGCCCCCT CTCCAAACTT CAGGCCACAG AGCTGGGGAC AAGGAGGCCA AAGTCCAGGA 960
ACATGACTCA CCCAGGGAAC AGGCCCAGCC TGCTGGCCAT AGTGGTGAGG GAGGCCAAGA 1020
GCCAAGAGGC CTGGGTTCCA GTCTGAGCTC CTCCAGGGCC AAGCTGGGTG ACCTTGGAGC 1080
AGCAGCTCAG CCTCTTTGGC TTCGGGGAGG GGGGAAGGGG CCGCAGTGAG AGAAGTGCCA 1140
GGGTCAGAAA GAAGAAGCTG AAGCTGGAGA CCAGCAGGCA GAACTTCAGG CCACAGAGGG 1200
CTCCAGCCCG CCTCCCCTGC TCCCCTGCTT CCTCACAAGG AACCTCATCT TCCTCATCTG 1260
TACAAAAGGG ACAAGAGTGC CAGCCTCATG AGACAAGGTA GCATAAAGTG GGCCGCTCCT 1320
CAAGAAATGG GAAGCTTCTG ATTGAAGAGA GGGAGAAATA GACTAAGAGA CTTGCCCAAG 1380
CCACAGAGCA AATTAGGATC AGCTGAACTC AGCCTCCATC TCCTGGCTCC CCACCTGGAG 1440
CTGTTTCTTT AAGACTGCTT GGAGGTCAAG TGTGGAGGGG GACAGGGGAG ATGTTGGGGT 1500
GTTGTTGGAT GCAGTGCCTC CCTGCCGCCC GATGAAGACC AATGAATCTG ATAGGAGTCC 1560
ACCATGCCCT ACCTTTACCC TAAACCCCAC TTGGCCCAAA GCTTGGACAA GAGGAGTGGC 1620
TCTAAGGGGA GGGAGGCACC CCACCTCCCA CCCCATCATG ACCAGCAGCA GCACCTGGTG 1680
CTTGGAAGGA CTAGAGGACC TGAGATGTCA GTGTCTAGGG CCCCTCGTTT TACAGGAGCC 1740
CAGAGAGGGA AAGGCCTAGC CTGAGGTCAC ACAGCACGAC AGCACAAGAG CCTAGAGTCC 1800
TGGCCACGGA CAGCCTCAGA GCAGAGTCCC CCTAGCCCCT GGGGGTGGCT GGAGCTGGGG 1860
GGCCCTGGGG GACTGAGTAA AGCGTGGCGA CAGATGGCCT GCCGAGGCAG CGGCGATCTG 1920
GGCGGCTGGC AGGCATGCTC GCTCCCGCGC AGGGAAGCGG CTAATTTTAG CTGAGGCCTC 1980
GATGCCAGCT TTGTTCCCCC CACCCACCCG CCGAGGGGGC CCAGCATGCC TTGCGTGCAA 2040
CCTGCCTCCC CCAGGCACCC CTACTCCCCC GCCTGGCCCC TTGGTGAGTA GTGCCCAGAC 2100
CCCAGGATCC 2110