EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-19698 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr3:5028210-5029080 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr3:5028516-5028528TGTCAGGGGGCG+7.22
Myod1MA0499.1chr3:5028340-5028353TGCAGCTGTCCCT+7.82
Number of super-enhancer constituents: 61             
IDCoordinateTissue/cell
SE_00456chr3:5017257-5029894Adipose_Nuclei
SE_00991chr3:5026988-5029313Adrenal_Gland
SE_01935chr3:5026848-5029303Aorta
SE_02322chr3:5026748-5029557Astrocytes
SE_03025chr3:5027381-5029274Bladder
SE_07573chr3:5018067-5029545Brain_Hippocampus_Middle_150
SE_09098chr3:5028379-5028625Brain_Mid_Frontal_Lobe
SE_09098chr3:5028900-5029032Brain_Mid_Frontal_Lobe
SE_09727chr3:5027360-5029781CD14
SE_12144chr3:5027817-5029256CD3
SE_13436chr3:5021106-5029476CD34_Primary_RO01536
SE_14396chr3:5017271-5031823CD4_Memory_Primary_7pool
SE_16423chr3:5027836-5029676CD4_Naive_Primary_8pool
SE_17173chr3:5024443-5029273CD4p_CD225int_CD127p_Tmem
SE_18090chr3:5017341-5029631CD4p_CD25-_CD45ROp_Memory
SE_19369chr3:5017800-5029439CD4p_CD25-_Il17p_PMAstim_Th17
SE_20043chr3:5017176-5029646CD56
SE_20744chr3:5017474-5031659CD8_Memory_7pool
SE_22663chr3:5024327-5029549CD8_primiary
SE_23149chr3:5027475-5029380Colon_Crypt_1
SE_24023chr3:5027525-5029214Colon_Crypt_2
SE_24955chr3:5028042-5029238Colon_Crypt_3
SE_25981chr3:5017485-5029777Duodenum_Smooth_Muscle
SE_26553chr3:5026679-5029464Esophagus
SE_27852chr3:5017792-5029567Fetal_Intestine
SE_28812chr3:5018045-5029449Fetal_Intestine_Large
SE_29870chr3:5024405-5031850Fetal_Muscle
SE_31556chr3:5026862-5029403Gastric
SE_34579chr3:5027474-5029410HCT-116
SE_34684chr3:5017233-5029863HeLa
SE_35840chr3:5020922-5029791HMEC
SE_36983chr3:5017322-5032227HSMMtube
SE_38020chr3:5017786-5030139HUVEC
SE_39863chr3:5026821-5031633K562
SE_40764chr3:5026743-5029556Left_Ventricle
SE_42278chr3:5026792-5029434Lung
SE_44737chr3:5026796-5030040NHDF-Ad
SE_45042chr3:5026791-5029524NHLF
SE_45785chr3:5017762-5030089Osteoblasts
SE_46992chr3:5028118-5029226Ovary
SE_47532chr3:5027418-5029302Pancreas
SE_48124chr3:5026803-5031698Psoas_Muscle
SE_48683chr3:5026847-5029428Right_Atrium
SE_49557chr3:5027476-5029115Right_Ventricle
SE_50324chr3:5026837-5029465Sigmoid_Colon
SE_51119chr3:5017007-5032856Skeletal_Muscle
SE_51934chr3:5024338-5029413Skeletal_Muscle_Myoblast
SE_52499chr3:5026830-5029459Small_Intestine
SE_53465chr3:5026782-5029450Spleen
SE_55004chr3:5024480-5029828Stomach_Smooth_Muscle
SE_55854chr3:5017401-5030090u87
SE_57258chr3:5027460-5029256VACO_400
SE_57799chr3:5027441-5029333VACO_503
SE_57996chr3:5028271-5029223VACO_9m
SE_61352chr3:5017379-5031549HBL1
SE_61694chr3:5013544-5031652Toledo
SE_62573chr3:5014508-5068965Tonsil
SE_63719chr3:5024338-5029427HSMM
SE_64232chr3:5020873-5029658NHEK
SE_65389chr3:5027023-5029590Pancreatic_islets
SE_67463chr3:5017401-5030090u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr350285345029013
Enhancer Sequence
GGAGTAGCTT TGGGGAAAGG AGGAAGTGGT TGGAGCAACC TGAACTAAAA AAAAAGATTT 60
GAGGGTTCCA CACACAGTCA ACCCAGAATC CCGCTATGGG AACCTGCCCC TGTCAAACAG 120
CGCCTCAAGT TGCAGCTGTC CCTCCACTTC ATTTTTTGCT TCCAGCTCGC CCTTAACCTC 180
TCTTCTAGCC CAGTTCTAGC GGCATCCAAA TGCGCTCAGA GGGAGGTGCG GGGGAGGGGC 240
GCGCACCCCA GCCTAATGCC CACTGCGGAC AAAGAGGACT TCTGTTTAAA AAGCGGGGTG 300
TGTGAGTGTC AGGGGGCGAA GCGCTGGCTC CGGGGCCAAG GAGAGGTGGC AGGAGGCAGG 360
GGAGCGGAGG CTGGGCATCT GGCCGCCTTC AGACAGGGCG TGATCCGCCG GGCCTGCCGG 420
GATGGTCTCA CCCAGCGCTG ACCTGCCCCG CCTGTTGACA CAACGTCACG TTTCCGACTG 480
CAGCCCTTTC ATGTGCGGCC CGCGGCTAAA AGCGGCTGCC GGTTCCTGGA AGCAGACGTG 540
CCTGGCACCG CGTCAGCAGA AACCTGATCC CCGGGGAAGC TCGGCAAGGC CTTGGGATCG 600
CTCGGCCCCC AGAACTAGGG CCTGGCAGCG GGCACGGGAC GCCCCCCCTC CCTCGCGCCC 660
AGCAGGAGGG AATTCGAGCG CTCCCCGTCG GCGGTGGGGA GGGAGGACTG GGTGGGGTAG 720
GGAGCTGGAT TTAGGCAGAG CACGGGGACC AGGGCTTAAT TGACTAGAAG CTAGAAGCTT 780
CCCACGGGTC ATCGCTCACT AATGCACGTC AAACAACCTA GAAGTATCAT TATGGGTACT 840
ATTACAATTC ACATTTTGTA GATAAATAAA 870