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

TagContent
EnhancerAtlas ID
HS154-11431 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr19:41316310-41318240 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs185308415chr1941317179hg19
rs4803370chr1941317934hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr19:41317048-41317059GCCCCGCCCCC+6.02
KLF5MA0599.1chr19:41317048-41317058GCCCCGCCCC+6.02
Klf12MA0742.1chr19:41316753-41316768GGCCACGCCCTATCC+6.37
SP1MA0079.4chr19:41317045-41317060TAGGCCCCGCCCCCA+6.73
SP2MA0516.2chr19:41317044-41317061TTAGGCCCCGCCCCCAT+6.29
SP4MA0685.1chr19:41317045-41317062TAGGCCCCGCCCCCATT+7.33
ZNF263MA0528.1chr19:41317350-41317371CCCCCAGCTCCCTCTTCCTTC-6.06
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_00640chr19:41315669-41318059Adipose_Nuclei
SE_01157chr19:41315730-41318064Adrenal_Gland
SE_03778chr19:41316136-41316712Brain_Angular_Gyrus
SE_03778chr19:41317046-41318179Brain_Angular_Gyrus
SE_04430chr19:41316025-41318437Brain_Anterior_Caudate
SE_05559chr19:41303199-41318218Brain_Cingulate_Gyrus
SE_06277chr19:41302932-41320507Brain_Hippocampus_Middle
SE_08430chr19:41305111-41319401Brain_Inferior_Temporal_Lobe
SE_09023chr19:41316786-41317117Brain_Mid_Frontal_Lobe
SE_09023chr19:41317319-41317521Brain_Mid_Frontal_Lobe
SE_12284chr19:41316412-41317472CD3
SE_14641chr19:41315407-41318311CD4_Memory_Primary_7pool
SE_17619chr19:41302314-41318336CD4p_CD25-_CD45RAp_Naive
SE_18094chr19:41316101-41318401CD4p_CD25-_CD45ROp_Memory
SE_20510chr19:41315981-41318457CD56
SE_21041chr19:41315661-41318057CD8_Memory_7pool
SE_22646chr19:41316051-41318156CD8_primiary
SE_24306chr19:41316137-41317756Colon_Crypt_2
SE_27495chr19:41315655-41317987Esophagus
SE_28298chr19:41315860-41318210Fetal_Intestine
SE_29113chr19:41315946-41318365Fetal_Intestine_Large
SE_31926chr19:41315546-41318078Gastric
SE_40037chr19:41315736-41317877K562
SE_41247chr19:41315084-41318145Left_Ventricle
SE_42595chr19:41315063-41318210Lung
SE_46944chr19:41316119-41318001Ovary
SE_50395chr19:41315142-41318493Sigmoid_Colon
SE_53239chr19:41315145-41318142Small_Intestine
SE_53554chr19:41315289-41318116Spleen
SE_65850chr19:41315830-41318292Pancreatic_islets
SE_69026chr19:41316097-41317794H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194131663641316800
Enhancer Sequence
GTCCCCATAG CGATAGCGGT TCCCGAAGAC AAGAACAGAT AACATTGGAT ACAGCATTAT 60
CCAGTAGCCG CACGGGGTCA AACGGGGCTC CTGGGGGTAG GAACAGGACG GTGGTCATAA 120
CGCGTGGTCC TGCCCCCAGC CAGCCCCATG GGCTTACTGG CTTTCTTCCA CCCAAATACC 180
TTCCAGTGGC CCCGTCTTGG CAGTGCAAGG GACTCTCCCA CACCAGGCCC TTCCGCTCTC 240
CCGGCCAGGC CGAAGCAATG GTGGCTTGAA ATTCGTCTAG CAGACAAGCC GCCTCCTCCA 300
GGACGCGCGC CTCGACGGTC CGCGTACCCA ACCCGAACTT CTTAAGCGCT CCAAGTGCAA 360
AATTGCGCAG TGTCCACCAG CACGGCCGGT TAGAAAACAA GATTCCTGTG GTGGGGACGG 420
GAAAGGAGGC GGGCCGGGGA GCCGGCCACG CCCTATCCAG GAAGCGCCGG GTCACTGGCT 480
ACATCCCTTT AGGGGCCTCC GACTCCTGCG GCCGGCTTCG TTCCCTTTGC TTCTTTACCA 540
GACCTCCAAG TGCCCTATCC ACACATTGGC CCCGCCTTTG CTGGGCTCCA TCCCTGACCT 600
AGGCTGGCTC TCGGGCTTTG ACTCTTAGGC TCTTTTCTCC TGTTGGCTGC AGGATGAACC 660
TCCATTCTAA CCTTACGCTT TAGCGCCGCC CCGCCCTCTC TCGGCCGTTT GCACCTCATT 720
AGCTGGAGTC TCTATTAGGC CCCGCCCCCA TTTGCCCGCC TCTACCATTT ACCCGCCCAG 780
CCTGGAGCGT CCGGGCCGGC AAGTCCAGCG CCGGGGCCTC ACTGTTTCCG CGTGTGAAGC 840
GTTCGAAGAC TGCCATGGAC CCGCGGCCAG AGACCGCATC CGCCTGTAGC ACTAACGCGT 900
CCCGCAGCGC TGCGTAGCCG CACAGCCCCA CCGCAGGGCG CGGGCCCAGC CGCACTGTGA 960
ACACCCGGCC CCAGCGGCCG GAGAGCTACG GGTAGCCGGT GCTCAGCGGG TGCCCATAGG 1020
GTTCCTCATC GGAGCCATTG CCCCCAGCTC CCTCTTCCTT CAGACCCAGG AGTCCTCGTC 1080
TCAGACCCTC ATTCCTCAGG CCCAGGAATT CAAATCCCCA GCTCCTTCCT CCCTGAGATC 1140
CAGGAGTCCA GGCCCCCACT TCCTTCTTCC CTTAGGACCT GGAAGTCCAG CTTCCCAGCC 1200
TCCTGCACCC TCAGAGTCGT CTCCTGGGCC CTCAGTACTC AGCCTGCCCA CCCTGAACCA 1260
GAACAGACCC CCTGCTCCCC TCTTCCCACA ACCTGATTTC CTGCTCTGGG CTCCTTCGTT 1320
ACGACCCAGT GTCCCGGCCC CAGGCTCTCC ACTCCCTATT CTCCTTTCCT AGTACTCAGC 1380
AGTCCGGAGC ACTCATCCTT CCTGTCCTTC CTCAGGATCA TAGAGTACAA ACCCTCAGCT 1440
GTCTTCATTC AGGAGGAGTT CTAGTCCCCA GCCCCACCTT CACGAATCCA GAATTCCGTT 1500
CCCCCATTCC TGTCGGGAAT GGAGTGCGCG GTCCAGGCCT CCGGACTGCA GCTGCAAGTT 1560
CCCCAGCAAT GGGAGCGGCC TGGGCCGGGG AGGTAGGGAC CCCCGCATCT GAGCGCGGCA 1620
CCCACCCTAC CCCCACCACG CCGGCGCCAG CACCAGAAGC CACAACAGCA GCGCAGCGAT 1680
ACCCGCGACA TGCCTGCAAT TCTCCACGCC TGCACCCCTT CACCTCTATT TGATTTCCAA 1740
GGGGTCTTAG GGGTGGAGCG GGGCGGAGAC CCGATGTGGG AGGAGTGGGC GTCTCCGGGC 1800
TGCTCATTCC GTGGATTCCC CAACCCGACG TCTCCACCCC GCCCCCAGCC CTAGTGGAGC 1860
TGTGCCCTGG CTCCCCCTGG CTTTTTTTGT GTGTCTGCCT CAGCCTGTCT TACTTAGCAA 1920
CTTTCGTGCA 1930