EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-47027 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr3:50636480-50639290 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat6MA0520.1chr3:50638655-50638670CAGTTCCTGAGAAGC+6.51
ZIC1MA0696.1chr3:50637318-50637332GGCCCCCTGCTGTG+7.38
ZIC3MA0697.1chr3:50637318-50637333GGCCCCCTGCTGTGG+6.16
ZIC4MA0751.1chr3:50637318-50637333GGCCCCCTGCTGTGG+6.34
Number of super-enhancer constituents: 41             
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_12583chr3:50638834-50639286CD34_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: 4             
ChromosomeStartEnd
chr35063737850637476
chr35063699650637093
chr35063835350638905
chr35063698550637600
Enhancer Sequence
CTCAAGTCAC GATGCAGGAT ACCTAGCTCT AGAACCACCT GCAGCAGGGC ACCGGTGTCC 60
CCTGCAAACC CATAGCTCTT TTCACTCAGG TCACGTGGGT CCCAGGTCAA CTTCATCCAC 120
AGCAGGTTCT TTCCAGCCAC AGCCAGCCTG ACCTGGGTGC AGGCATCAAG GCCTCTAAGT 180
GACAGAGAAT GCAGCACTCC CACCCACTGC CAGCTGCCCC AGGTAGCTTC TGAGAACTGG 240
CCACTGCAGA GTACAAGCAC AGCAATGACC TGTGTCCTTG GGCTGCCCCA CTGCCCTCCT 300
ACAGGGGAGG GAGGACCTCT CTGCCATAGC CCCACCTCAC AGCTGCCACC CACCCACTGG 360
GTCCTAGCCC TTCTTAACGC CAGCATTGTC CCCATCTTCT CTGTGACATT GGGGTGGATG 420
GGTAGCACGC TTGGCGCTGT GCTCAGTGAG GGCCAAGGAG TGACCTGAGG GTGGGAGGAG 480
AGAGGCAAGT TCTTGCCGAC ACCCCGTCCA GCCTTGGCCA GGGGAGGTTC TCCATTCTGA 540
AGGTAAAGGG GTCATGAGTG GTTAAAAGGT TGTCCTAGTG CCTCCCAGCT ATGTGACCCT 600
GACCTGCTCA CTCAGCACCC TCAGCCATAC TTCCAGGCCC CTGCTCTAAC AATGCTGCTC 660
CTGGGATCCT GTGATGGGAA CACTCATGGC CATTCCCTTG AAATGTGGCC AGACTTCAAC 720
CCAGTCCCAG ACAGTTGTCA GTGCCCACTC ACTGCAGCCT CTCCTCTGCA TTCTCCAGGC 780
TATTTTCCAA AAGGCCAGAT GCATGTCCTG GGTGGCTTGA TGCTGAAGCT GGGGCCTGGG 840
CCCCCTGCTG TGGGACAGGG AAGTGTGGGT GAGACAAGGC TGTCCTGAAG GAGTGACTAG 900
AGCCAGAGGC TGCCCACCAG CAAAGGGGGC TCAGTGAGCA GGGCCTGGCA CTGCTGACCC 960
CACCTTGTTT TCCCTCCTAC TCTCCCTTGG TGCTTCACAC CCCCGGCTGC TCACTGGCCT 1020
AGGCAGGACA CTCCTGTCTA ACCTCCTGCT TTCACTGTGG ACCCACACCC ACACGCTGCC 1080
TCCATAGGTA CACATGCCCT TTTTTTCTCT ACTAACACCT GTTTCTCGTC GTCCACTCTG 1140
CCAGGCTGGA CACCGGGCAC TTCAGAGGTC ATGCCAGATC CAGCACCGGG ATGGAGGAGT 1200
CTAAGGAGGC ACCTGCAGTC AGGGAGGGCT TCCTGGAGGC AGAGACCGAA GCTAAGGGCT 1260
CAGTACCCTC TCCCCCCACT TACCCCAGGT CACTGGCTGT CCTCTGAGCC TCACTCCCTG 1320
GAAGGGCCAG CAGGTTCCAG GAAGTGTCCC CTCGCCCTGC AGTGCTGGTT CCAAGAACTG 1380
CAGCTCTTGG CAGCATTTGC TTAGGATCCT TTCCTAGAAC TTGAGACCTG CTCTGCCCAG 1440
ACTGCTGGGG TCTCAGAGGG CAGCCAGTGG GGGTAGTGGG GGAAGGGGGT GCACTGGGAG 1500
GTGCCTCTGC AGGTAGAACA TTCCATGGAC CAAACATTGG GAGGTGGGCC TAGGCTGTCA 1560
GCCGGGAGTG GTTGGCCACA CTAGGGTGGT CAACACCTCC AACAGGAGGT CGGTGAAATG 1620
CAGGTGCTTT GACTGCAGTC AACCATGGGG TGCGGGCCCA TGAGTTCTCC CTGCACAAGA 1680
AGGAGGCTCA TTCCCTTGGT CCAGAACTTC CACCAGCTTG CCACATGCCA CCCTCCACCC 1740
CCCGACTCTA CTCCCCCCAC TAGCCTGGCA CCAGGGTCCC ATCCCATAGA GAATCAGCAC 1800
AGGCCTTACC CTCAGAATAG GCCCTCATCA GATAACCTCC AGAGGACAGG CCAGGGTGCA 1860
GGACAGGCAG GTTCTGAGCA GGGAAGGGGG ATGGGATCGT CTTGGGGCCC TTGGAAGGCC 1920
ATGACACTTG TGTTATTAAT CCTGTTATAA TTTTACCTTT CCTGGTTAGA ACTGAATAAA 1980
TTACCCCACC TCACACCCCC CAGCAAAGTT GGGTCGGGTG AATGAGGGAC AGGCCCTGGT 2040
AAGTGGTCAA GGACAGGGCC CTACTTCCCT CAAGGTCACC AGGCCTCCCC CTGGGGCGTG 2100
TCCTCCACCC GCCACTTCTG AGCTGGCACC AGGCCTGCCC AGCCGCCTGG GACCTGCCAG 2160
ATCACGTTGA GCAACCAGTT CCTGAGAAGC GTTGAAGGCA GTGTGGTTTA AAATTAACTC 2220
CCCCGCTCCC CCTCCCGCCT GCGGCCTCCT CTGAGTTCTT GGAAGCGGCG CTCTGCTCTT 2280
CCTGGGAAGA GGCCTCCAGC CCCAGCTGCT GCAATTCTGG CGAAAACACC TCACCCAGGC 2340
TGGGGGTGGG GGGTGCCCAC GCCAGGCCTT CTCTGCCCTA CACAAGGCCC AGGGATCCTC 2400
TGGAAGCTAG CACCCACCCT AGTTACTCAC TGAGACCCAG AAGAGAAAGG GGGTGATTGT 2460
CAAGGTGCTG GGAGGAGGTG CTCCTGCCCC CAAAGCCCAC AGCTCCCAAC CAGGCACCTC 2520
TGGGTAGGAG AGAAAGTGAA TTGATCCCAC AACAGCAAAC CCAGGACCCT GGCCTACTTT 2580
GAGCCATATA TGTCCTGGCG AGATGCAGCA ACTTCCTAGG GCCACCCAGC TTTGCCTGCC 2640
CTTATAAGCT CAGCTTGCCC ACTAGGTGCC AGGCTGATGG TGCTGATCTG GCAAGGATGC 2700
CCGGGAGCAC GCCCCCGCAG GCATGCACAC ACCTGGGTTA ACAGTGATCT CTGCCAGGAT 2760
CTCTCCTTTT CTCTCACCCA CACCCCTCAA ACTGCCCTTG GAACACCTCT 2810