EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-27891 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr19:39209080-39211780 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TFAP2AMA0003.3chr19:39211461-39211472TGCCTGAGGCA-6.02
Number of super-enhancer constituents: 47             
IDCoordinateTissue/cell
SE_00117chr19:39209697-39211399Adipose_Nuclei
SE_00865chr19:39209014-39211789Adrenal_Gland
SE_01543chr19:39209086-39216749Aorta
SE_03166chr19:39209126-39214577Brain_Angular_Gyrus
SE_03903chr19:39208114-39214876Brain_Anterior_Caudate
SE_04868chr19:39207314-39215407Brain_Cingulate_Gyrus
SE_05805chr19:39207187-39220624Brain_Hippocampus_Middle
SE_06803chr19:39208167-39215131Brain_Hippocampus_Middle_150
SE_07777chr19:39206500-39216075Brain_Inferior_Temporal_Lobe
SE_08790chr19:39209326-39210032Brain_Mid_Frontal_Lobe
SE_08790chr19:39210069-39210556Brain_Mid_Frontal_Lobe
SE_08790chr19:39210761-39211324Brain_Mid_Frontal_Lobe
SE_08790chr19:39211404-39211723Brain_Mid_Frontal_Lobe
SE_23062chr19:39209159-39210693Colon_Crypt_1
SE_23732chr19:39209251-39210916Colon_Crypt_2
SE_24739chr19:39209210-39211611Colon_Crypt_3
SE_26525chr19:39209025-39214484Esophagus
SE_27614chr19:39208366-39214814Fetal_Intestine
SE_28533chr19:39209007-39214316Fetal_Intestine_Large
SE_29583chr19:39209014-39214267Fetal_Muscle
SE_31384chr19:39209121-39215258Gastric
SE_34299chr19:39209103-39211350HCT-116
SE_35812chr19:39209139-39211932HMEC
SE_36926chr19:39204544-39214311HSMMtube
SE_40594chr19:39209040-39215024Left_Ventricle
SE_42097chr19:39206714-39214813Lung
SE_44161chr19:39209000-39210799NHDF-Ad
SE_45660chr19:39209068-39211365Osteoblasts
SE_46686chr19:39210107-39210515Ovary
SE_47114chr19:39164477-39226374Panc1
SE_47461chr19:39209318-39209984Pancreas
SE_47461chr19:39210031-39210730Pancreas
SE_47461chr19:39210765-39211306Pancreas
SE_48075chr19:39209081-39214283Psoas_Muscle
SE_48555chr19:39206718-39215387Right_Atrium
SE_49449chr19:39209231-39209783Right_Ventricle
SE_49449chr19:39209805-39211192Right_Ventricle
SE_50056chr19:39209142-39211532Sigmoid_Colon
SE_51136chr19:39209189-39214563Skeletal_Muscle
SE_51705chr19:39208981-39211838Skeletal_Muscle_Myoblast
SE_52339chr19:39209135-39211571Small_Intestine
SE_53291chr19:39208993-39215023Spleen
SE_54534chr19:39209632-39211366Stomach_Smooth_Muscle
SE_56725chr19:39209127-39211909VACO_400
SE_57359chr19:39209179-39210978VACO_503
SE_63494chr19:39209005-39211843HSMM
SE_65266chr19:39208442-39214408Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr193920924639211374
Number: 1             
IDChromosomeStartEnd
GH19I038717chr193920829539214866
Enhancer Sequence
TGGGAGGATT GATTGAGCCA GGGAGGTCAA GGCTGCAGTG AGCCGTGATT GTACCACTGC 60
ACTCCAGCCT GGGTGACAGA GCAAGACCCT GTCTCAAAAA AAAAGGAAAG AAATGCTGCT 120
TTGGATTCCT TCAGCCCCAG AAAGCAGGGA CCATTCAGGG GCCAGGTCCT CTTTGTTGCC 180
CAGTCTGCCC TCGCCTCAGA GGTGGGACCC TGTCAGTCAT CCAGGAACAC AGCCAAGCCC 240
CCTCCAGCAC TTCAGGGAAG TGACCTTACA CCCATCTGTT TGTCCCCTCT GCGTGTCTTC 300
CCCATCCAGG GCGAGTGTGT GGGGCAGGCC TCTTCCATCC CCCGCACCCT GTGTTCAGAG 360
TCGGCTTCCC TCTCCCACAC CTCTGTGAGC GTGGACGGAA GGCTGGGGAG CCCATGTTCA 420
CTGGCACGTC CCTCAGGCTA GAGGAGGGCC TGCCTCCTGG GCCTGCTGCC GGACCACAGC 480
CAGTGCTCAC CCTCAGACAG TGCTCACCCA CTGCCTTCGG CCCACCCTTC AGCATGGCCC 540
ACCTGTGAGC TCCTCCCACC TCCCATCCCT TCCCAGAGCC TCCTTCCCGG GCCTGGCTCC 600
CCCTGCAGGA GCGCCACTGT GCTTTCTGTT CTCGGCAGCC CTGCAGCTGC CTGGCCGTTG 660
GCTCCAGATG TGGGATTTCA TCACGTCCCT GGCCCTCTTT TGGGTCATGC CAAGGTTGAG 720
ATTTCAGATC CCAGGGGTCT GGAAGCCTTC AGAAAGCTGC CAGTGCCTGG GAGAGCCACA 780
AGAGCCACTC ACAGGACTCC TCTCCCACTC TGGCCACCAC CTTCCCAACA CAGTCTCCCT 840
GGCCCTCCGG CCGCCACTCC GCCCAGCTGA GCCCTTCCTT GCATTCCTGA GTGCATTTTC 900
TCACCCCTCC CCACCCTGGC CCGCATGCGA GTGTGCAGCT CCACACGGCC TGCAGCCCTG 960
GCCACGGCCC AGCTTGTGCC CTCCTCACAT GAGCTCAGCT CGCCATTCCC GCGGCAGCTG 1020
CCAGCCTCAG AGCAGCCCAG CCCCTTTGCT ACCAGGAAAG AGTGCGAGTG AGAGAGTGGA 1080
TAGTGAGGGA GGAAGGGCCT GGCCAGGCCG GGTGCCGCAC TTCCCTCTTG CCTGGCAGAA 1140
AGGCACCCAT GTGAGGAGAG CGTGTTAGCA CCGATGCCAT CTTGTGTGGT TGGTGGCCTC 1200
CATCCATTCC CGGATTCACT CATTCGTTCA ACAGACAGCT CAGGTGGCTC CAGCCGTCCT 1260
TATCCATGGA GGCCTGGGCG TCGCCCTGTG GCTGAACCTT CTGGGGGTCT TTCTGCCCAC 1320
CCATCAGCTC TTCAGTCCCT CTACAGGGCT CCATGAGGCC CTGCAGATGG TTTCCTGAGG 1380
CCAAGGGGCT GGGTGTGGTG GCCCCACTGG CATTCCTCCC CTGGGAAGGG CTCTGGGGCA 1440
GCCTTCACCT GAGGTGTTTA GAAGCCAGCT CAGTCTCCGG CCAGGGCCCA GCTGGTTCAG 1500
CGGCCTCCAC ACGTCCCTGC CCCACCCCTA CCTGACTGGG CATCCACGCG GGTCTGCCCA 1560
TGGCGTCTGC CAGAGCCCCC AGGCAGGCTG GCCTACTAAT TCCCAAGACT CAGAGCCTCT 1620
GTCCTCTCAA GTAGCAGTTA CGTGAAACAG GACAGGCAGG CCCTCCACAC CCCAGGGTCT 1680
GGTCGTAGCG GCCTCCTCCG CCCTGGGGTG GGTGGGCCAC CTTCACTCCA CACCCCTCAC 1740
CATCCCCCAC AGCCCGCAGC GGGAGGGTCG TCGTGGATGC TTCTCTGAGG GACTTGATTT 1800
CCTGGGAATA CGACCAACCC CGAACGACCC CTTGTCCCCA CTCCAGTTGT CCCTTGGCCT 1860
GGATCCCAGA TAGCTGTGGC AATGGTCCGC TGCCCACATC CTCTCGGTGC ACCCTTGCCA 1920
GGACTCTGCG GAGGCAGAGG GAGATGTCAC CTGCTGTTTC TGGTTCCTGC CCCTGGGAGA 1980
AAGCAGTTGG AGAAGGGAAT TGCAAGGCCG CCTTGTGGCT GAGCCTCCTG CCCCAGGGCT 2040
GCGCAGCAGG GCCGGTGGAG CCAGAGTCTC CCAGGCCTCC CACTTCTTGG CCATCAGTGC 2100
CAGAGCCGAT CCTGTGGGGA GTCTGGTAGG TGCCTGACAG TTGAGACTGG GAGAGGCTGA 2160
GGTGAGGCTG GTACTGGCTC CATGCCTGCT GTGCTCGAAC ACCACCTCAC TGAAACTTGA 2220
GAATAGTTCC ATGCCACACA GGTACTGGGG CTGGCCCCAT TTTACAGATG AAGGCACAGG 2280
CCCAGAGAGG CCTCGGTGGC TGCACTGGGC GGGCAGCTGT CAGGTGCTGG GACAGAGCTG 2340
AGGGGATCTC CGCTACCACT TGGGGGAAGC CCAAGGTGGT GTGCCTGAGG CAGGGCCCCT 2400
GTAGGAGCTG GGGTGCAGCC ACCTTCCCAG GCTGGCATTT TCCCTGCGGT TCCCTAAAGA 2460
CCTTCACTTG CTTGCAGGGC TTCCTTGAGC TTTGGTTCTG GGATGTGTAA TTAGCCAGGA 2520
TCAGGGACTA ATAACAGCGT TCCTCCTTTC CTTTAAAGGG CCTGATGGTG GGCCCGCCCC 2580
AATGCACACA GGACACCTTA GGACAGCGTG GGGCACTTAG ACGTGGAGAG GACCACCACC 2640
TGTGCGGGTG CAGGGTCAGG GTCCTAGAAG AAGCTGGCTC TGATGCTTCC CCTTCCCCAA 2700