EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS094-26865 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr3:50637870-50639290 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat6MA0520.1chr3:50638655-50638670CAGTTCCTGAGAAGC+6.51
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00760chr3:50636720-50645111Adipose_Nuclei
SE_09279chr3:50636789-50643770CD14
SE_12298chr3:50637567-50641454CD3
SE_12583chr3:50637855-50638154CD34_adult
SE_12583chr3:50638231-50638567CD34_adult
SE_12583chr3:50638569-50638827CD34_adult
SE_12583chr3:50638834-50639286CD34_adult
SE_12919chr3:50637190-50639496CD34_Primary_RO01480
SE_13361chr3:50636482-50651600CD34_Primary_RO01536
SE_14184chr3:50637803-50641619CD34_Primary_RO01549
SE_14601chr3:50635365-50652110CD4_Memory_Primary_7pool
SE_15705chr3:50637773-50640862CD4_Memory_Primary_8pool
SE_16238chr3:50637562-50640385CD4_Naive_Primary_7pool
SE_16582chr3:50637829-50640336CD4_Naive_Primary_8pool
SE_17166chr3:50637926-50640703CD4p_CD225int_CD127p_Tmem
SE_18495chr3:50635603-50652144CD4p_CD25-_Il17-_PMAstim_Th
SE_19130chr3:50636430-50651976CD4p_CD25-_Il17p_PMAstim_Th17
SE_20626chr3:50637316-50651753CD56
SE_20911chr3:50636515-50652055CD8_Memory_7pool
SE_23649chr3:50636580-50642032Colon_Crypt_1
SE_23932chr3:50636606-50641027Colon_Crypt_2
SE_25135chr3:50636534-50641205Colon_Crypt_3
SE_25369chr3:50635253-50654453DND41
SE_26772chr3:50636910-50645175Esophagus
SE_27877chr3:50636977-50641548Fetal_Intestine
SE_28892chr3:50636927-50641567Fetal_Intestine_Large
SE_30531chr3:50636456-50641120Fetal_Muscle
SE_31573chr3:50636327-50646177Gastric
SE_40028chr3:50636324-50651737K562
SE_40824chr3:50635650-50651738Left_Ventricle
SE_42458chr3:50635760-50651762Lung
SE_47024chr3:50636967-50638655Ovary
SE_47024chr3:50638661-50639495Ovary
SE_47758chr3:50636646-50641285Pancreas
SE_48262chr3:50636469-50651773Psoas_Muscle
SE_49250chr3:50636324-50643972Right_Atrium
SE_49448chr3:50636552-50640884Right_Ventricle
SE_50378chr3:50636461-50651683Sigmoid_Colon
SE_51369chr3:50636562-50644163Skeletal_Muscle
SE_52764chr3:50636819-50646284Small_Intestine
SE_53704chr3:50636516-50641543Spleen
SE_65451chr3:50636456-50645477Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr35063835350638905
Enhancer Sequence
CAGCATTTGC TTAGGATCCT TTCCTAGAAC TTGAGACCTG CTCTGCCCAG ACTGCTGGGG 60
TCTCAGAGGG CAGCCAGTGG GGGTAGTGGG GGAAGGGGGT GCACTGGGAG GTGCCTCTGC 120
AGGTAGAACA TTCCATGGAC CAAACATTGG GAGGTGGGCC TAGGCTGTCA GCCGGGAGTG 180
GTTGGCCACA CTAGGGTGGT CAACACCTCC AACAGGAGGT CGGTGAAATG CAGGTGCTTT 240
GACTGCAGTC AACCATGGGG TGCGGGCCCA TGAGTTCTCC CTGCACAAGA AGGAGGCTCA 300
TTCCCTTGGT CCAGAACTTC CACCAGCTTG CCACATGCCA CCCTCCACCC CCCGACTCTA 360
CTCCCCCCAC TAGCCTGGCA CCAGGGTCCC ATCCCATAGA GAATCAGCAC AGGCCTTACC 420
CTCAGAATAG GCCCTCATCA GATAACCTCC AGAGGACAGG CCAGGGTGCA GGACAGGCAG 480
GTTCTGAGCA GGGAAGGGGG ATGGGATCGT CTTGGGGCCC TTGGAAGGCC ATGACACTTG 540
TGTTATTAAT CCTGTTATAA TTTTACCTTT CCTGGTTAGA ACTGAATAAA TTACCCCACC 600
TCACACCCCC CAGCAAAGTT GGGTCGGGTG AATGAGGGAC AGGCCCTGGT AAGTGGTCAA 660
GGACAGGGCC CTACTTCCCT CAAGGTCACC AGGCCTCCCC CTGGGGCGTG TCCTCCACCC 720
GCCACTTCTG AGCTGGCACC AGGCCTGCCC AGCCGCCTGG GACCTGCCAG ATCACGTTGA 780
GCAACCAGTT CCTGAGAAGC GTTGAAGGCA GTGTGGTTTA AAATTAACTC CCCCGCTCCC 840
CCTCCCGCCT GCGGCCTCCT CTGAGTTCTT GGAAGCGGCG CTCTGCTCTT CCTGGGAAGA 900
GGCCTCCAGC CCCAGCTGCT GCAATTCTGG CGAAAACACC TCACCCAGGC TGGGGGTGGG 960
GGGTGCCCAC GCCAGGCCTT CTCTGCCCTA CACAAGGCCC AGGGATCCTC TGGAAGCTAG 1020
CACCCACCCT AGTTACTCAC TGAGACCCAG AAGAGAAAGG GGGTGATTGT CAAGGTGCTG 1080
GGAGGAGGTG CTCCTGCCCC CAAAGCCCAC AGCTCCCAAC CAGGCACCTC TGGGTAGGAG 1140
AGAAAGTGAA TTGATCCCAC AACAGCAAAC CCAGGACCCT GGCCTACTTT GAGCCATATA 1200
TGTCCTGGCG AGATGCAGCA ACTTCCTAGG GCCACCCAGC TTTGCCTGCC CTTATAAGCT 1260
CAGCTTGCCC ACTAGGTGCC AGGCTGATGG TGCTGATCTG GCAAGGATGC CCGGGAGCAC 1320
GCCCCCGCAG GCATGCACAC ACCTGGGTTA ACAGTGATCT CTGCCAGGAT CTCTCCTTTT 1380
CTCTCACCCA CACCCCTCAA ACTGCCCTTG GAACACCTCT 1420