EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS104-29746 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr19:41315630-41317690 
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
Number: 1             
IDChromosomeStartEnd
GH19I040810chr194131554141315690
Enhancer Sequence
CACCTGCCAC CTCTAGGTAC TTAAGCAGAA TGAGGAGCCC ATAGCACAGG GTGGTGCTCG 60
TGGTTTCGGT GACGCCAAAA AAAAAATGCG TCGTCATTAC CGACGTCTAC TCCTGGAAAT 120
GGCTCTCCGG GTCCTGCTGT TACTGTGGGC AGAGGAGATG TGCTGCCGCG TGCCAGGCAC 180
CTGTTGGTGG GCGGCATGGA TAGAGTTTAG AGAGCTGGGA CCCATGCCTT ACCCATCTGG 240
TCAAGCAATC AATGAAATCG CGGGGCTCCG CTGGCTGCCG CATCTGCCAG TGTCGTTGAA 300
TTTGCTCAGA GATGACCCGC AGCTCCGAAA AGTTTCGGAA GATTCGGTGG TGCGGGCCCG 360
GGAGCCAGTC CATGAGGGAC AGGCAAATGT ACATCTGGAG AGACAGGGTC TGTCTCAACA 420
TGGGCCCTGC ACAAGGCCAC TAGGCCTTAG TTTCCCTACA GGGAGATTGG ACTAGGACTT 480
TGATACTGGA TGTTCTAGAA CTCTTCCAGG AATCTGTCCC ATTCTAATGA TCCATTGTAG 540
GTAGGTCTGT GTACTCGGGA TTTGGCATAA GGCTGGACGC ACCAAGGAAA GATTGTGGCC 600
GGCCCTCTCA CCTCGCCCCA TCTGGAACTA ATGATGCAGA AGTTGTCACT GAAGAGGTTC 660
AGGAGCCTCA GGAACTCCGG GTCCCCATAG CGATAGCGGT TCCCGAAGAC AAGAACAGAT 720
AACATTGGAT ACAGCATTAT CCAGTAGCCG CACGGGGTCA AACGGGGCTC CTGGGGGTAG 780
GAACAGGACG GTGGTCATAA CGCGTGGTCC TGCCCCCAGC CAGCCCCATG GGCTTACTGG 840
CTTTCTTCCA CCCAAATACC TTCCAGTGGC CCCGTCTTGG CAGTGCAAGG GACTCTCCCA 900
CACCAGGCCC TTCCGCTCTC CCGGCCAGGC CGAAGCAATG GTGGCTTGAA ATTCGTCTAG 960
CAGACAAGCC GCCTCCTCCA GGACGCGCGC CTCGACGGTC CGCGTACCCA ACCCGAACTT 1020
CTTAAGCGCT CCAAGTGCAA AATTGCGCAG TGTCCACCAG CACGGCCGGT TAGAAAACAA 1080
GATTCCTGTG GTGGGGACGG GAAAGGAGGC GGGCCGGGGA GCCGGCCACG CCCTATCCAG 1140
GAAGCGCCGG GTCACTGGCT ACATCCCTTT AGGGGCCTCC GACTCCTGCG GCCGGCTTCG 1200
TTCCCTTTGC TTCTTTACCA GACCTCCAAG TGCCCTATCC ACACATTGGC CCCGCCTTTG 1260
CTGGGCTCCA TCCCTGACCT AGGCTGGCTC TCGGGCTTTG ACTCTTAGGC TCTTTTCTCC 1320
TGTTGGCTGC AGGATGAACC TCCATTCTAA CCTTACGCTT TAGCGCCGCC CCGCCCTCTC 1380
TCGGCCGTTT GCACCTCATT AGCTGGAGTC TCTATTAGGC CCCGCCCCCA TTTGCCCGCC 1440
TCTACCATTT ACCCGCCCAG CCTGGAGCGT CCGGGCCGGC AAGTCCAGCG CCGGGGCCTC 1500
ACTGTTTCCG CGTGTGAAGC GTTCGAAGAC TGCCATGGAC CCGCGGCCAG AGACCGCATC 1560
CGCCTGTAGC ACTAACGCGT CCCGCAGCGC TGCGTAGCCG CACAGCCCCA CCGCAGGGCG 1620
CGGGCCCAGC CGCACTGTGA ACACCCGGCC CCAGCGGCCG GAGAGCTACG GGTAGCCGGT 1680
GCTCAGCGGG TGCCCATAGG GTTCCTCATC GGAGCCATTG CCCCCAGCTC CCTCTTCCTT 1740
CAGACCCAGG AGTCCTCGTC TCAGACCCTC ATTCCTCAGG CCCAGGAATT CAAATCCCCA 1800
GCTCCTTCCT CCCTGAGATC CAGGAGTCCA GGCCCCCACT TCCTTCTTCC CTTAGGACCT 1860
GGAAGTCCAG CTTCCCAGCC TCCTGCACCC TCAGAGTCGT CTCCTGGGCC CTCAGTACTC 1920
AGCCTGCCCA CCCTGAACCA GAACAGACCC CCTGCTCCCC TCTTCCCACA ACCTGATTTC 1980
CTGCTCTGGG CTCCTTCGTT ACGACCCAGT GTCCCGGCCC CAGGCTCTCC ACTCCCTATT 2040
CTCCTTTCCT AGTACTCAGC 2060