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

TagContent
EnhancerAtlas ID
HS060-00709 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr1:27888970-27890430 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr1:27890271-27890282GCTTCCCGCCC-6.02
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00527chr1:27889462-27891915Adipose_Nuclei
SE_00861chr1:27886075-27904718Adrenal_Gland
SE_01588chr1:27886149-27904879Aorta
SE_02913chr1:27887486-27889346Bladder
SE_02913chr1:27890049-27890615Bladder
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_08953chr1:27889480-27889882Brain_Mid_Frontal_Lobe
SE_14757chr1:27885672-27892439CD4_Memory_Primary_7pool
SE_23479chr1:27888886-27895065Colon_Crypt_1
SE_24168chr1:27889383-27892160Colon_Crypt_2
SE_24711chr1:27888433-27889356Colon_Crypt_3
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: 2             
ChromosomeStartEnd
chr12788901927889666
chr12788972427889774
Number: 1             
IDChromosomeStartEnd
GH01I027559chr12788613127905256
Enhancer Sequence
AGGGACACAG CCCCCTGCCT CCCATGCAAA CCCTGCCTTG GTGCCCCACC TCACAGACAC 60
ACACCTGCCC TGGCCCTAAA GGCCCTTCTC CACACCATCT GAAGAATGCT GGGTCCCTCC 120
CCCTGGGGAA CAGTCCCACG GGCTGACATA TGGGTGAGAG GGTAGATCAT GCGGGACTGA 180
GCACCCCCCA GCTCCCACTT GTCCCTCTGC TCAGGGCCCT AAGCATTTCC TCTGGCCAGC 240
CCTTTGGGGC TCTGTGGTCT GCATGGGAAG GCCCCACCAG CTGCCAGCCC CGTATCACCA 300
GAAAACATGT CGTCTCTTTA GAGTGAGACA CGAGCTCCCA AGTTACTGAC AACTTCCCAA 360
CAGCATGAGA GAATCACACA TGCCACTCCC CACAACAGCC TGCGACGGGC ACATGGTGAC 420
ATCTCACACA CACAACAGCC AGAGACAGGC GCACAAGTTG GTGACAACCC TCCTAACGGG 480
ATGAACTAAG CACATAACCT GTCGCTTCCT CCAAACATGA GATGGGCACA CCTGACACAC 540
CCTCGACAGC ATGGGGCAGG CGTCTGTTAC CCCTCACAGT GGCATAACTG ACACGCAACC 600
AGGCACCCCC ACACCCACTA ATGCACAGAG AACCTGTTAC ACAGCTGACC AAGACACACA 660
CACACGCACG CACGCATGCA TGCACACACC CACACAAAGA ACCTGTCACA TAGTTGACCA 720
AGACACACAC ACATGCACAC ACACACAGAA CCTGTCACAC AGCTGACCAA GACACACACA 780
CACGCACGCA TGCATGCACA CACCCACACA AAGAACCTGT CACATAGTTG ACCAAGACAC 840
ACACACATGC ACACACACAC AGAACCTGTC ACACAGCTGA CCAAGACACA CACACACACA 900
CACACACACG TGGGACAAGT CCCATCTTCC AGGTGTGAGG AAGGCATGGA CCCCTCCACC 960
CACCACACAG CATGAGGCAG GGACATAACC TCGCCCCTGC CTGGGAATCC TCCCTGCAGA 1020
CTGTGGGATG GGTACACAAC ATGTCACCTC CCCGGCTGCC TTGGACAGGT GACAGCCCAC 1080
CTCACCCCTC CCCCATCACT GTCACCAGCC TGGGTGGTGC CGTCCCTCTG CCTGCAGAGG 1140
CGTCACAGCT CACACGGCAT GAATGTCACC CCAGCACTGC CAGAGCCGGG CACAGCCACA 1200
CATTGCCCCA GTGACAAACA CCACTGGCCC CAGAGGAGGT GAAGGCACAC AGGGCTCTGG 1260
TGTGACCTTG GCCTCTGGAC ACCAGGAGGG GAGGTGCTGT GGCTTCCCGC CCAGTGGCGG 1320
GTGCTGGGGG AGAGGAGTGC TGGGGAGGAA GCTGCCTGGA CACACTGACT ACCTGGAAAT 1380
GCCACCTCCC CCAGCCCTCA CTCCACTCCA TTTCTTATTC ACTGTAGTTG TGTATCTAGG 1440
GAGGGGGCTG AATGAGTGGT 1460