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

TagContent
EnhancerAtlas ID
HS180-01021 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:27889790-27891670 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr1:27890271-27890282GCTTCCCGCCC-6.02
HNF4GMA0484.1chr1:27890632-27890647GGAGGCCAAAGTCCA+7.22
Hnf4aMA0114.3chr1:27890633-27890649GAGGCCAAAGTCCAGG+6.26
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: 2             
ChromosomeStartEnd
chr12788986027891017
chr12788980027891375
Number: 1             
IDChromosomeStartEnd
GH01I027559chr12788613127905256
Enhancer Sequence
CACATAGTTG ACCAAGACAC ACACACATGC ACACACACAC AGAACCTGTC ACACAGCTGA 60
CCAAGACACA CACACACACA CACACACACG TGGGACAAGT CCCATCTTCC AGGTGTGAGG 120
AAGGCATGGA CCCCTCCACC CACCACACAG CATGAGGCAG GGACATAACC TCGCCCCTGC 180
CTGGGAATCC TCCCTGCAGA CTGTGGGATG GGTACACAAC ATGTCACCTC CCCGGCTGCC 240
TTGGACAGGT GACAGCCCAC CTCACCCCTC CCCCATCACT GTCACCAGCC TGGGTGGTGC 300
CGTCCCTCTG CCTGCAGAGG CGTCACAGCT CACACGGCAT GAATGTCACC CCAGCACTGC 360
CAGAGCCGGG CACAGCCACA CATTGCCCCA GTGACAAACA CCACTGGCCC CAGAGGAGGT 420
GAAGGCACAC AGGGCTCTGG TGTGACCTTG GCCTCTGGAC ACCAGGAGGG GAGGTGCTGT 480
GGCTTCCCGC CCAGTGGCGG GTGCTGGGGG AGAGGAGTGC TGGGGAGGAA GCTGCCTGGA 540
CACACTGACT ACCTGGAAAT GCCACCTCCC CCAGCCCTCA CTCCACTCCA TTTCTTATTC 600
ACTGTAGTTG TGTATCTAGG GAGGGGGCTG AATGAGTGGT GGAGGGAGGG CTGTCCTGAG 660
GCGCTGTTAC TATGAGACTG CTTAGAGATC AGTGGGGAGT AGGGCGGTTA GGGGTTGCTA 720
TCACCATGTG CTCAGTGGGA AGAGTATGGG ATAATGGCTT GAGACCCCCA TAGCTTCCAG 780
GGGAGCCCTT CTTCCTTACA AAGGCCCCCT CTCCAAACTT CAGGCCACAG AGCTGGGGAC 840
AAGGAGGCCA AAGTCCAGGA ACATGACTCA CCCAGGGAAC AGGCCCAGCC TGCTGGCCAT 900
AGTGGTGAGG GAGGCCAAGA GCCAAGAGGC CTGGGTTCCA GTCTGAGCTC CTCCAGGGCC 960
AAGCTGGGTG ACCTTGGAGC AGCAGCTCAG CCTCTTTGGC TTCGGGGAGG GGGGAAGGGG 1020
CCGCAGTGAG AGAAGTGCCA GGGTCAGAAA GAAGAAGCTG AAGCTGGAGA CCAGCAGGCA 1080
GAACTTCAGG CCACAGAGGG CTCCAGCCCG CCTCCCCTGC TCCCCTGCTT CCTCACAAGG 1140
AACCTCATCT TCCTCATCTG TACAAAAGGG ACAAGAGTGC CAGCCTCATG AGACAAGGTA 1200
GCATAAAGTG GGCCGCTCCT CAAGAAATGG GAAGCTTCTG ATTGAAGAGA GGGAGAAATA 1260
GACTAAGAGA CTTGCCCAAG CCACAGAGCA AATTAGGATC AGCTGAACTC AGCCTCCATC 1320
TCCTGGCTCC CCACCTGGAG CTGTTTCTTT AAGACTGCTT GGAGGTCAAG TGTGGAGGGG 1380
GACAGGGGAG ATGTTGGGGT GTTGTTGGAT GCAGTGCCTC CCTGCCGCCC GATGAAGACC 1440
AATGAATCTG ATAGGAGTCC ACCATGCCCT ACCTTTACCC TAAACCCCAC TTGGCCCAAA 1500
GCTTGGACAA GAGGAGTGGC TCTAAGGGGA GGGAGGCACC CCACCTCCCA CCCCATCATG 1560
ACCAGCAGCA GCACCTGGTG CTTGGAAGGA CTAGAGGACC TGAGATGTCA GTGTCTAGGG 1620
CCCCTCGTTT TACAGGAGCC CAGAGAGGGA AAGGCCTAGC CTGAGGTCAC ACAGCACGAC 1680
AGCACAAGAG CCTAGAGTCC TGGCCACGGA CAGCCTCAGA GCAGAGTCCC CCTAGCCCCT 1740
GGGGGTGGCT GGAGCTGGGG GGCCCTGGGG GACTGAGTAA AGCGTGGCGA CAGATGGCCT 1800
GCCGAGGCAG CGGCGATCTG GGCGGCTGGC AGGCATGCTC GCTCCCGCGC AGGGAAGCGG 1860
CTAATTTTAG CTGAGGCCTC 1880