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

TagContent
EnhancerAtlas ID
HS105-40275 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr19:41315700-41317920 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs185308415chr1941317179hg19
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: 30             
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_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
GACGCCAAAA AAAAAATGCG TCGTCATTAC CGACGTCTAC TCCTGGAAAT GGCTCTCCGG 60
GTCCTGCTGT TACTGTGGGC AGAGGAGATG TGCTGCCGCG TGCCAGGCAC CTGTTGGTGG 120
GCGGCATGGA TAGAGTTTAG AGAGCTGGGA CCCATGCCTT ACCCATCTGG TCAAGCAATC 180
AATGAAATCG CGGGGCTCCG CTGGCTGCCG CATCTGCCAG TGTCGTTGAA TTTGCTCAGA 240
GATGACCCGC AGCTCCGAAA AGTTTCGGAA GATTCGGTGG TGCGGGCCCG GGAGCCAGTC 300
CATGAGGGAC AGGCAAATGT ACATCTGGAG AGACAGGGTC TGTCTCAACA TGGGCCCTGC 360
ACAAGGCCAC TAGGCCTTAG TTTCCCTACA GGGAGATTGG ACTAGGACTT TGATACTGGA 420
TGTTCTAGAA CTCTTCCAGG AATCTGTCCC ATTCTAATGA TCCATTGTAG GTAGGTCTGT 480
GTACTCGGGA TTTGGCATAA GGCTGGACGC ACCAAGGAAA GATTGTGGCC GGCCCTCTCA 540
CCTCGCCCCA TCTGGAACTA ATGATGCAGA AGTTGTCACT GAAGAGGTTC AGGAGCCTCA 600
GGAACTCCGG GTCCCCATAG CGATAGCGGT TCCCGAAGAC AAGAACAGAT AACATTGGAT 660
ACAGCATTAT CCAGTAGCCG CACGGGGTCA AACGGGGCTC CTGGGGGTAG GAACAGGACG 720
GTGGTCATAA CGCGTGGTCC TGCCCCCAGC CAGCCCCATG GGCTTACTGG CTTTCTTCCA 780
CCCAAATACC TTCCAGTGGC CCCGTCTTGG CAGTGCAAGG GACTCTCCCA CACCAGGCCC 840
TTCCGCTCTC CCGGCCAGGC CGAAGCAATG GTGGCTTGAA ATTCGTCTAG CAGACAAGCC 900
GCCTCCTCCA GGACGCGCGC CTCGACGGTC CGCGTACCCA ACCCGAACTT CTTAAGCGCT 960
CCAAGTGCAA AATTGCGCAG TGTCCACCAG CACGGCCGGT TAGAAAACAA GATTCCTGTG 1020
GTGGGGACGG GAAAGGAGGC GGGCCGGGGA GCCGGCCACG CCCTATCCAG GAAGCGCCGG 1080
GTCACTGGCT ACATCCCTTT AGGGGCCTCC GACTCCTGCG GCCGGCTTCG TTCCCTTTGC 1140
TTCTTTACCA GACCTCCAAG TGCCCTATCC ACACATTGGC CCCGCCTTTG CTGGGCTCCA 1200
TCCCTGACCT AGGCTGGCTC TCGGGCTTTG ACTCTTAGGC TCTTTTCTCC TGTTGGCTGC 1260
AGGATGAACC TCCATTCTAA CCTTACGCTT TAGCGCCGCC CCGCCCTCTC TCGGCCGTTT 1320
GCACCTCATT AGCTGGAGTC TCTATTAGGC CCCGCCCCCA TTTGCCCGCC TCTACCATTT 1380
ACCCGCCCAG CCTGGAGCGT CCGGGCCGGC AAGTCCAGCG CCGGGGCCTC ACTGTTTCCG 1440
CGTGTGAAGC GTTCGAAGAC TGCCATGGAC CCGCGGCCAG AGACCGCATC CGCCTGTAGC 1500
ACTAACGCGT CCCGCAGCGC TGCGTAGCCG CACAGCCCCA CCGCAGGGCG CGGGCCCAGC 1560
CGCACTGTGA ACACCCGGCC CCAGCGGCCG GAGAGCTACG GGTAGCCGGT GCTCAGCGGG 1620
TGCCCATAGG GTTCCTCATC GGAGCCATTG CCCCCAGCTC CCTCTTCCTT CAGACCCAGG 1680
AGTCCTCGTC TCAGACCCTC ATTCCTCAGG CCCAGGAATT CAAATCCCCA GCTCCTTCCT 1740
CCCTGAGATC CAGGAGTCCA GGCCCCCACT TCCTTCTTCC CTTAGGACCT GGAAGTCCAG 1800
CTTCCCAGCC TCCTGCACCC TCAGAGTCGT CTCCTGGGCC CTCAGTACTC AGCCTGCCCA 1860
CCCTGAACCA GAACAGACCC CCTGCTCCCC TCTTCCCACA ACCTGATTTC CTGCTCTGGG 1920
CTCCTTCGTT ACGACCCAGT GTCCCGGCCC CAGGCTCTCC ACTCCCTATT CTCCTTTCCT 1980
AGTACTCAGC AGTCCGGAGC ACTCATCCTT CCTGTCCTTC CTCAGGATCA TAGAGTACAA 2040
ACCCTCAGCT GTCTTCATTC AGGAGGAGTT CTAGTCCCCA GCCCCACCTT CACGAATCCA 2100
GAATTCCGTT CCCCCATTCC TGTCGGGAAT GGAGTGCGCG GTCCAGGCCT CCGGACTGCA 2160
GCTGCAAGTT CCCCAGCAAT GGGAGCGGCC TGGGCCGGGG AGGTAGGGAC CCCCGCATCT 2220