EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-17594 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr19:41315430-41318360 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs185308415chr1941317179hg19
rs4803370chr1941317934hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr19:41317048-41317059GCCCCGCCCCC+6.02
KLF5MA0599.1chr19:41317048-41317058GCCCCGCCCC+6.02
Klf12MA0742.1chr19:41316753-41316768GGCCACGCCCTATCC+6.37
SNAI2MA0745.2chr19:41318269-41318279AACAGGTGCA+6.02
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
Number: 1             
IDChromosomeStartEnd
GH19I040810chr194131554141315690
Enhancer Sequence
GCACTGGATC TCGAGCAGCA CTGCGTTGGC GTAGGGCAGG CACACGCGAT AGTCCAGGCT 60
TGGGGCGGGC CTCCACCCTA CCACAGGGTC CAGCTCCTGC ACCTTGGCTC AGGCCGGGGG 120
AGGCTGTGAG CTGCGCACTT CCAGGACCCT CCAGCCATCC CCAGACTGCA GCCTCCCATT 180
CTGGGTCTCT CCGGGTTGCA CACCTGCCAC CTCTAGGTAC TTAAGCAGAA TGAGGAGCCC 240
ATAGCACAGG GTGGTGCTCG TGGTTTCGGT GACGCCAAAA AAAAAATGCG TCGTCATTAC 300
CGACGTCTAC TCCTGGAAAT GGCTCTCCGG GTCCTGCTGT TACTGTGGGC AGAGGAGATG 360
TGCTGCCGCG TGCCAGGCAC CTGTTGGTGG GCGGCATGGA TAGAGTTTAG AGAGCTGGGA 420
CCCATGCCTT ACCCATCTGG TCAAGCAATC AATGAAATCG CGGGGCTCCG CTGGCTGCCG 480
CATCTGCCAG TGTCGTTGAA TTTGCTCAGA GATGACCCGC AGCTCCGAAA AGTTTCGGAA 540
GATTCGGTGG TGCGGGCCCG GGAGCCAGTC CATGAGGGAC AGGCAAATGT ACATCTGGAG 600
AGACAGGGTC TGTCTCAACA TGGGCCCTGC ACAAGGCCAC TAGGCCTTAG TTTCCCTACA 660
GGGAGATTGG ACTAGGACTT TGATACTGGA TGTTCTAGAA CTCTTCCAGG AATCTGTCCC 720
ATTCTAATGA TCCATTGTAG GTAGGTCTGT GTACTCGGGA TTTGGCATAA GGCTGGACGC 780
ACCAAGGAAA GATTGTGGCC GGCCCTCTCA CCTCGCCCCA TCTGGAACTA ATGATGCAGA 840
AGTTGTCACT GAAGAGGTTC AGGAGCCTCA GGAACTCCGG GTCCCCATAG CGATAGCGGT 900
TCCCGAAGAC AAGAACAGAT AACATTGGAT ACAGCATTAT CCAGTAGCCG CACGGGGTCA 960
AACGGGGCTC CTGGGGGTAG GAACAGGACG GTGGTCATAA CGCGTGGTCC TGCCCCCAGC 1020
CAGCCCCATG GGCTTACTGG CTTTCTTCCA CCCAAATACC TTCCAGTGGC CCCGTCTTGG 1080
CAGTGCAAGG GACTCTCCCA CACCAGGCCC TTCCGCTCTC CCGGCCAGGC CGAAGCAATG 1140
GTGGCTTGAA ATTCGTCTAG CAGACAAGCC GCCTCCTCCA GGACGCGCGC CTCGACGGTC 1200
CGCGTACCCA ACCCGAACTT CTTAAGCGCT CCAAGTGCAA AATTGCGCAG TGTCCACCAG 1260
CACGGCCGGT TAGAAAACAA GATTCCTGTG GTGGGGACGG GAAAGGAGGC GGGCCGGGGA 1320
GCCGGCCACG CCCTATCCAG GAAGCGCCGG GTCACTGGCT ACATCCCTTT AGGGGCCTCC 1380
GACTCCTGCG GCCGGCTTCG TTCCCTTTGC TTCTTTACCA GACCTCCAAG TGCCCTATCC 1440
ACACATTGGC CCCGCCTTTG CTGGGCTCCA TCCCTGACCT AGGCTGGCTC TCGGGCTTTG 1500
ACTCTTAGGC TCTTTTCTCC TGTTGGCTGC AGGATGAACC TCCATTCTAA CCTTACGCTT 1560
TAGCGCCGCC CCGCCCTCTC TCGGCCGTTT GCACCTCATT AGCTGGAGTC TCTATTAGGC 1620
CCCGCCCCCA TTTGCCCGCC TCTACCATTT ACCCGCCCAG CCTGGAGCGT CCGGGCCGGC 1680
AAGTCCAGCG CCGGGGCCTC ACTGTTTCCG CGTGTGAAGC GTTCGAAGAC TGCCATGGAC 1740
CCGCGGCCAG AGACCGCATC CGCCTGTAGC ACTAACGCGT CCCGCAGCGC TGCGTAGCCG 1800
CACAGCCCCA CCGCAGGGCG CGGGCCCAGC CGCACTGTGA ACACCCGGCC CCAGCGGCCG 1860
GAGAGCTACG GGTAGCCGGT GCTCAGCGGG TGCCCATAGG GTTCCTCATC GGAGCCATTG 1920
CCCCCAGCTC CCTCTTCCTT CAGACCCAGG AGTCCTCGTC TCAGACCCTC ATTCCTCAGG 1980
CCCAGGAATT CAAATCCCCA GCTCCTTCCT CCCTGAGATC CAGGAGTCCA GGCCCCCACT 2040
TCCTTCTTCC CTTAGGACCT GGAAGTCCAG CTTCCCAGCC TCCTGCACCC TCAGAGTCGT 2100
CTCCTGGGCC CTCAGTACTC AGCCTGCCCA CCCTGAACCA GAACAGACCC CCTGCTCCCC 2160
TCTTCCCACA ACCTGATTTC CTGCTCTGGG CTCCTTCGTT ACGACCCAGT GTCCCGGCCC 2220
CAGGCTCTCC ACTCCCTATT CTCCTTTCCT AGTACTCAGC AGTCCGGAGC ACTCATCCTT 2280
CCTGTCCTTC CTCAGGATCA TAGAGTACAA ACCCTCAGCT GTCTTCATTC AGGAGGAGTT 2340
CTAGTCCCCA GCCCCACCTT CACGAATCCA GAATTCCGTT CCCCCATTCC TGTCGGGAAT 2400
GGAGTGCGCG GTCCAGGCCT CCGGACTGCA GCTGCAAGTT CCCCAGCAAT GGGAGCGGCC 2460
TGGGCCGGGG AGGTAGGGAC CCCCGCATCT GAGCGCGGCA CCCACCCTAC CCCCACCACG 2520
CCGGCGCCAG CACCAGAAGC CACAACAGCA GCGCAGCGAT ACCCGCGACA TGCCTGCAAT 2580
TCTCCACGCC TGCACCCCTT CACCTCTATT TGATTTCCAA GGGGTCTTAG GGGTGGAGCG 2640
GGGCGGAGAC CCGATGTGGG AGGAGTGGGC GTCTCCGGGC TGCTCATTCC GTGGATTCCC 2700
CAACCCGACG TCTCCACCCC GCCCCCAGCC CTAGTGGAGC TGTGCCCTGG CTCCCCCTGG 2760
CTTTTTTTGT GTGTCTGCCT CAGCCTGTCT TACTTAGCAA CTTTCGTGCA CCAGCATTTT 2820
CATGGCAACA CACCTGGACA ACAGGTGCAC CCTCCTGAGC CCCTAGCACC TTTGAGTCCA 2880
ATTTACTTGG CCTGTAAGTG TGTATTCCTC AATCTCCGGG CCACCTCTGG 2930