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

TagContent
EnhancerAtlas ID
HS051-13782 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:13187040-13189420 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:13187650-13187668GGGAGGAGGAAAGGAGGG+6.04
ZfxMA0146.2chr19:13188826-13188840CCCGGCTAGGCCTG+6.08
Znf423MA0116.1chr19:13188591-13188606GGCCCCCTGGGGGCC-6.76
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00024chr19:13186400-13187475Adipose_Nuclei
SE_00024chr19:13188702-13190936Adipose_Nuclei
SE_01540chr19:13185912-13191032Aorta
SE_03137chr19:13185943-13189489Brain_Angular_Gyrus
SE_03859chr19:13178766-13190754Brain_Anterior_Caudate
SE_04986chr19:13170672-13191599Brain_Cingulate_Gyrus
SE_05848chr19:13160560-13191529Brain_Hippocampus_Middle
SE_06678chr19:13160758-13191322Brain_Hippocampus_Middle_150
SE_07717chr19:13170719-13191634Brain_Inferior_Temporal_Lobe
SE_08780chr19:13187203-13188148Brain_Mid_Frontal_Lobe
SE_08780chr19:13188154-13188398Brain_Mid_Frontal_Lobe
SE_08780chr19:13188438-13189138Brain_Mid_Frontal_Lobe
SE_12503chr19:13187603-13187877CD34_adult
SE_12503chr19:13188820-13189068CD34_adult
SE_26520chr19:13186737-13191429Esophagus
SE_29770chr19:13186804-13191144Fetal_Muscle
SE_31390chr19:13187255-13191052Gastric
SE_33451chr19:13186648-13194806H2171
SE_40665chr19:13187476-13191190Left_Ventricle
SE_41557chr19:13186975-13190958LNCaP
SE_44148chr19:13186767-13188177NHDF-Ad
SE_44148chr19:13188761-13191143NHDF-Ad
SE_44758chr19:13187607-13188422NHLF
SE_46667chr19:13186973-13187366Ovary
SE_46667chr19:13187379-13187716Ovary
SE_46667chr19:13188476-13189294Ovary
SE_48143chr19:13185896-13191050Psoas_Muscle
SE_48559chr19:13188390-13191183Right_Atrium
SE_51076chr19:13188612-13190819Skeletal_Muscle
SE_54519chr19:13186440-13191599Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191318826413188490
Number: 1             
IDChromosomeStartEnd
GH19I013076chr191318703713191536
Enhancer Sequence
CAGCTTCACA GAGAGAGGCT CAGAGTCTAG TGAAGAATGA GCAGAGTCCT TTTGAGACCA 60
GGTAGGGAAG CTAGCGAAGG GGAGAGAGTA CAGAGGAAGC CAGCTCAGAC CTTCCCAGTC 120
TCCTCTAGGG ATCTTCTTCT TGTTGAACCC ACCCCCCTTC ACCTCCATTC TTGACTGAGG 180
GTGCAGACAG ACCTAGAGAG GACTCTGGAA GACAGCATGT AACACGTGCG TGTGTGTGTG 240
TGCATGTGCA TGAGCACATG TGTGTGAGGA GGCTGGCCGC AAGAGTCCCC CGCTGACGTG 300
CCAGTGGTAC AGCCCGTGTT TATCCTCACT GTGGGTGTGA CAGGGCCTGG GAGTGCAGAC 360
TCACGCGTGT GGGTTGTGCA CAGGGCATGG CTGCTCTGGA CAGGCCTGGG CCCTGGGCAT 420
CATTCTCCTC CTCCAAAAGG TGAGGGTCTG ACCTAATGGT ACTTTGTCTG ATGTTTTCCA 480
GATATGCCCC TACTGGGAAG GGCCAAGTGG GCAGGCAGAG TCTGGGGTGG AGCGAGGTGG 540
GGCTGGGAAG CACTCCTGCT TTTCTGCTGC CCCAGAACGA ATGCAAGTTC TGGCAGCTTC 600
TCCTCCTCCT GGGAGGAGGA AAGGAGGGCT CGCCTCCAGG CCTCAGGCTG AGGGAGTGGG 660
CTGGAGACCC TCTAGATGGC CAGCAGAGGC TGGCCTCTGT GAGAAGGCTT CCTTGCGTGA 720
CTCTGGGGCC CCTCCCAGGC TCTCCTCGTG GCAGGCAGGG ACTTGGGCCA GCATGGGCCA 780
CATGCTTCCC TAGGGGAGCC TTGAGAGGCA GAGAGAGGAG TTGAGAAGGC CCGGGAGACT 840
CTTGGGCTAC ATCCTGGGTC CCTGGCCGGG GCCTCAGTAG GTGACCCCTT CTGCAAGGAC 900
TGCCCCTGGG GTGCATAGAG GACTGTGTCT GCAGCTGGCT CCTGGGGCAA GGGCTCCTGG 960
GCTCCTGTGC CCAGACCTAA TTCCTGAGGA GCCCCCCTCT TCCTGGCTCC TGCTCTCTCC 1020
TTTCTTGGCT GTCTGCTTTT GCGCCTGCCA TTTCTGCATT TCTGCTCCTT CCGGCAGTCC 1080
TGCCACGCAC GGCCCCTCAA CATCCTCCTG CAGCACCCTC CGGCTCCCTT TTCCCCTCAC 1140
CCCGCTGTGT GTTGTTTTCA TGGGCTGCAA CAAATTGCCA ATTAAGCAGC CCAGCTGCAG 1200
GACAGGGAAC AGCTGGGGAG GCACTGTGCG GCCATGGGGA CAGCTGTGCA CAGCTGGTAG 1260
GATGCTCCCC CCTCCCCACT GTGCCAGCTA TCAGGTGGCA CACAGCTGCT GCCAGATAAC 1320
ACCTCCGCTG GCGGCTGGGA GTTCGCCCTT CCCCCGCCCC TTCCCTCTGC AGTTAAGATG 1380
GCTCTTTATT TCTCTGTTCT GCAGCCCCTC CACCCCTCAC CCAAACTGAC TTGATTTGTC 1440
CTCCAAGGGT GGCAGCTGTG AGATCTGCCC CAACTCTACC TTATCCTTCC CAGCCTGGGC 1500
ACAACCTTAA AGCTCAGCCC AAGATGGGAG CTGATCTTTC CAGAAGAACC TGGCCCCCTG 1560
GGGGCCCTGC TTTGTCATTT GGATGCTATG GCCACTGGGC AGAGATGAAT TTCTAAAGAC 1620
AGACTTCAAA CAAGGTGTTC TCTGTGCCCT TGTTTCATGC TGAATGCCAC CCACACCTCT 1680
GGCACCAGAA GCAGGGCAGA GCCCTGAAAT TATCCATCCT ATGGCAGCTG AGCTTCTGGG 1740
TCCCCTGGCT GGGGGAGTCT TCTCCCCTCT GGCTCTGCCT GCACAGCCCG GCTAGGCCTG 1800
AGCAGCCCAA GGACTCTCCA GGTCCTCTGG CCTCTGTCCC TGCTCTCTCG CTGGGCATTG 1860
TGTCCCTCCT GAGGGCTCAT GGCTGTGTGC TCCCTTCCCT AAACGGGGCC CTGGCTTCTT 1920
CCCACCAGAA CCTCCCATGG CCCCGGGCAC CATGGCATAG ACCCCAGCCT GTCCCTCCCA 1980
AACTTACCCC TTCCCGGCTC TCAAGCTGGC GCCCTGGGGT TCCTCCTGCA CTCCTTTCCC 2040
AATGTTGGTC CTGCATCCCA CCCTTTCACT TCATTACCTG CTTGCCAGGG CATAGGCTGG 2100
GGCCCTTGCT CACCCCCTGC CTGGCACACA CCACCCCACA TTACCCAGGG GCCTCGTTTT 2160
CCTCTCTGGT TAGAAGCACC CCTTGGCTGG CCTACACACA GGGCCTCGGA ACCAGGCCTA 2220
GAACAAGGCC TGGGACTGGG CAAGGAGCAG CAGGAGGGAG CACAGTGGAG GAAGGGGCAG 2280
TGGGGAGGGG CTGAGGAGAG AAGGAGCGAG CTGCTGGCTT CCCGCCTTCC CCGCACCCAC 2340
CCCAGCCCAG CTAAACCTGC CCTGTGTTGC TGCTTCCTCC 2380