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

TagContent
EnhancerAtlas ID
HS018-13993 
Organism
Homo sapiens 
Tissue/cell
CD19+ 
Coordinate
chr20:25018340-25019960 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6050267chr2025019099hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF2MA0051.1chr20:25018824-25018842GGAAAGTGAAAGTCTCTT+6.18
ZNF263MA0528.1chr20:25019622-25019643TCCCTCCCCTGCCCCTCCTCC-7.77
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_01860chr20:25017701-25021723Aorta
SE_03453chr20:25017710-25019265Brain_Angular_Gyrus
SE_03453chr20:25019320-25021482Brain_Angular_Gyrus
SE_04126chr20:25016146-25021701Brain_Anterior_Caudate
SE_05098chr20:25016289-25026626Brain_Cingulate_Gyrus
SE_05867chr20:25009884-25041019Brain_Hippocampus_Middle
SE_06947chr20:25008932-25026827Brain_Hippocampus_Middle_150
SE_08089chr20:25015965-25026562Brain_Inferior_Temporal_Lobe
SE_08927chr20:25018757-25018950Brain_Mid_Frontal_Lobe
SE_08927chr20:25019039-25019321Brain_Mid_Frontal_Lobe
SE_11633chr20:25015552-25028126CD20
SE_23688chr20:25017698-25021595Colon_Crypt_1
SE_24056chr20:25017780-25020014Colon_Crypt_2
SE_25265chr20:25017710-25019730Colon_Crypt_3
SE_27084chr20:25017735-25021719Esophagus
SE_29549chr20:25018015-25019244Fetal_Intestine_Large
SE_29549chr20:25019674-25021615Fetal_Intestine_Large
SE_30760chr20:25017959-25018862Fetal_Muscle
SE_30760chr20:25019497-25021753Fetal_Muscle
SE_31460chr20:25017655-25021710Gastric
SE_40636chr20:25016197-25021763Left_Ventricle
SE_41962chr20:25017724-25020051LNCaP
SE_42209chr20:25016477-25021748Lung
SE_47497chr20:25017799-25018933Pancreas
SE_47497chr20:25019007-25021557Pancreas
SE_48726chr20:25017715-25021736Right_Atrium
SE_49493chr20:25018255-25021555Right_Ventricle
SE_50687chr20:25017729-25021565Sigmoid_Colon
SE_51643chr20:25016516-25022884Skeletal_Muscle
SE_52650chr20:25017716-25021718Small_Intestine
SE_54397chr20:25018123-25020883Spleen
SE_54979chr20:25017519-25024711Stomach_Smooth_Muscle
SE_59947chr20:25013726-25040720Ly4
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr202501908725019137
chr202501838425018988
Number: 1             
IDChromosomeStartEnd
GH20I025035chr202501571425021830
Enhancer Sequence
CCTTAGGGAA GGGAAGCCTG GCGAGGCTGA CCCCTTCTCA CGCAGGAGGA GCGTGGAAGG 60
CCACGCAAAG CATGGATGGC CAGCTCGCAT CTCATGGACC CAGGCCTGGG GAACAGACTC 120
CTTCCCTCCT GGCAGCCTCC TCTGGCCCTG ACATTACTGT AGCCACTGAC TGTCATTCAA 180
TGGTGGTAAG ATTTGCTCAC TCTGCTGAGA GAACAGAAGA CCAGGAAGTC AGCTAGCAGG 240
GCTCATAAAC CAAGTATGAA ATTTCTCACG TCATTATTTG ATGTCATGAC CATGACATTT 300
AGCAAAGAGA AGCTGCCGTG AAAACATAAA GTGGCAGCCG CACTTGAACA TGAATGGTCC 360
CCTGGGCCAA GGCGGGCCCA GGCACAGCGA GGGCCCCCAG GAGACATGAG CTGAGTTGCT 420
AGTAGTGATG CCAGCTCAGC CAGTAACAAG ATCACTAAAG CTATGTGTGT TCTAAATTCC 480
TTATGGAAAG TGAAAGTCTC TTCCCTGAGG TTTTGCTAGA CTCTGTGGAA AGCGCTGAAC 540
CTGCAAGTTT ATCACTCAGG AGTCTCACGG GAGGCCAAAC AATGACTGAT CAGAGAGCAG 600
GGTTCCCAAC ACAGCCCCCC ACACCACTGG GGCCTGAACT GTCTCATCTG TGAAATGGCC 660
TAATAATAGG ACCCACTACC AAGGTGGTCG TGGAGACCAA ATATGAAGTT GCAGGCACCT 720
TTGAAGGTGA CCTGTAAACA GTGGCCATAA TGACTGCAGA AAATACAAGA CATGGGAAAA 780
AGAGAATTAT TGAACACTGA TGGACCTTTA AGAAAGGTGG GCACCTCAGG CACCTCCTTC 840
TCAGGAGGGC AGGTGCAAAA TGCTGGTTTG CCTTATGGAA GCTGCAGTCT CCGTGTCGCC 900
GGCTCAGGGC ACATGCACCT CAGCTGTGTG AATGCCTTGC AGGAAGCCCT CACCTGCACA 960
GCCTGCCTGC TCCATGCCCC CAAGGCAGGT GCTGAGGGCG GGAGTAGATC TGAGAAGGAT 1020
GCAGAGCCTC CTACAGTTGG GGTTGCTGCC AGTCTGGGGG TTCCAGGCAC TCAGCCCGAG 1080
GCCTGTGCTT CCAAAAGGCC AGAGGGAAGG CAGTTCCACC CCACATGCTC TGCACAGCCT 1140
ACCACCATCT GCCATGTCGT CCTGTCACTG CCCCCCTGCT GGCTACCCAA GCTTCTCCAG 1200
CCATGATTGC CTGCCACTGC CAGCACAGGA AACCTCCTCT CCAGGCCCAT GGCCTCCTAC 1260
CTCCTCTGCA TCCAGGGGGT ATTCCCTCCC CTGCCCCTCC TCCCACTTGT CCTCACCCCA 1320
CCCTCAGTTC ACAGCCCCAT CCCATGGAAC AAGGACAGAA CAGCTATCAA GCAAGTATCC 1380
TGTACCCAGG GCTGCTCCCA CAGAGCAGGT TCCCATGGAG AACCCACTTA ACCCTCACAA 1440
CAGCCCATAG GTTCTGAGCT CCCCTTCCCT TCTTCACTTT CCTGATGAGG AAATTGAGGC 1500
ATAGAGAAGT TGGGCCACTT TCTCAAGGCT ATTCAGCTGA AGGAGTCAGG GCAGGATTCA 1560
AACCCAGGCC CAGCTCCAGG GGCCTTGCTG TCAGCCAGCT CCTCAGTATC AGAACCACTC 1620