EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-04489 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr1:234851090-234852840 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs496800chr1234851216hg19
rs553427chr1234852760hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ETV6MA0645.1chr1:234852460-234852470AGCGGAAGTG+6.02
MEF2AMA0052.3chr1:234851902-234851914ACTAAAAATAGA+6.27
MEF2BMA0660.1chr1:234851902-234851914ACTAAAAATAGA+6.32
MEF2CMA0497.1chr1:234851900-234851915CTACTAAAAATAGAA+6.57
NFAT5MA0606.1chr1:234851106-234851116AATGGAAAAT-6.02
NFATC1MA0624.1chr1:234851106-234851116AATGGAAAAT-6.02
NFATC3MA0625.1chr1:234851106-234851116AATGGAAAAT-6.02
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_01816chr1:234851920-234853206Aorta
SE_03123chr1:234851948-234853100Bladder
SE_04206chr1:234851848-234864664Brain_Anterior_Caudate
SE_05210chr1:234852339-234866021Brain_Cingulate_Gyrus
SE_06159chr1:234851621-234865554Brain_Hippocampus_Middle
SE_07154chr1:234851931-234854072Brain_Hippocampus_Middle_150
SE_08108chr1:234852036-234868294Brain_Inferior_Temporal_Lobe
SE_23501chr1:234850856-234854176Colon_Crypt_1
SE_24081chr1:234850921-234851933Colon_Crypt_2
SE_24081chr1:234851981-234853206Colon_Crypt_2
SE_25941chr1:234850948-234863804Duodenum_Smooth_Muscle
SE_26800chr1:234850930-234853175Esophagus
SE_27714chr1:234849701-234863899Fetal_Intestine
SE_28624chr1:234846479-234863924Fetal_Intestine_Large
SE_29677chr1:234852242-234854916Fetal_Muscle
SE_31598chr1:234850948-234853235Gastric
SE_33532chr1:234851300-234853496H2171
SE_40926chr1:234850897-234863890Left_Ventricle
SE_42335chr1:234851052-234854297Lung
SE_45839chr1:234850144-234851437Osteoblasts
SE_47205chr1:234850913-234851958Panc1
SE_47205chr1:234851968-234863960Panc1
SE_48724chr1:234850971-234851902Right_Atrium
SE_48724chr1:234851922-234853176Right_Atrium
SE_50295chr1:234850736-234862837Sigmoid_Colon
SE_51414chr1:234851031-234863972Skeletal_Muscle
SE_52508chr1:234850914-234854694Small_Intestine
SE_54175chr1:234851139-234851896Spleen
SE_54631chr1:234850764-234864075Stomach_Smooth_Muscle
SE_61992chr1:234850904-234881356Toledo
SE_63435chr1:234845326-234887436NCI-H69
SE_65556chr1:234851662-234853082Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1234851967234852444
Number: 1             
IDChromosomeStartEnd
GH01I234714chr1234849979234864746
Enhancer Sequence
GGGGCCACCA AAACATAATG GAAAATGCCC ACCACACACT ACACGCTTCT TCATTACATT 60
GGCTCAATAC TGAGAATGAC CGCACAGGAC AGCCCTCTTG CATGACACTA AGGTTTTGTA 120
GGTGAACTGC CACCTGTTAG ATTTCCACTT CCTTTGTTCT CCTACAGTGA GGTCTTTGTC 180
CTGAGTTGAG GGGAGGACAG ATTTTGGTGG GAAGATGATC TGAGTTTAAA GGGGCTCTGA 240
GAGATCCACA TGCAGCTGTC TAGTAGGTTA ATGGGAATAC CCATCCAACA CTCTGGAAAG 300
AGGTCCTTGC TGGAGATGGA AATCTAGGGT CCTTCACATT GGCATGGTTG TTGGAACCAC 360
GGCTGGGTCA GAGTTGTTGA GGAGCACAGA CCTCTGAAGG GGGAAGAACA AGGAACCTTG 420
GGAGCACCGA TAATTGCTGG ATACACGAGC TCTGCGACAG GAAGGCAAGC ATAAGGCTGT 480
CATGCCATAA AAACTAAGGC AAGAGAGAGT TTCCATGCGA GGGAGGGGTC ACACGAACTG 540
AATACAGTCC AAAGGACTGT AGGCAGTGGA TGATACTATT TAGGAGGTCT AAATATAGCT 600
CTAGTAATCT CAGCAAGAAT AAGTTACAAT GAAACAATTA CGGGTAAGGG AGAAGCTAGC 660
TAGATTTCAC TGGACTAAAA AGGAGTAAGA AAGGAGTGGC TGGGCACCAT GGCTCACGTC 720
TGTAATCCCA GCACTTTGGA AGGCTGAGGC AGGCGGGTCA CGAGGTCAAC AGATCGAGAC 780
CATCCGGGTG AACATAGTGA AACCCTGTTT CTACTAAAAA TAGAAAAACT AGCTGGGCGT 840
GGTAGCGCAT GCCTGTAATC CCAGCTACTC GGGAGGCTGA GGCAGGAGAA TCACTTGAAC 900
CCGGGAGGCA GAGGTTGCAG TGAGCCGAGA TCATGCCATT ATTGCACTCC AGCCTGGCGA 960
CAGCTAGAGA CTCTGTCTCA AGAAAAGAAA AAAAAAGAAA GAAAGAAAGG AGTAAATGGT 1020
GCCAGCAAGA TAGCTACATA GAATGGAAAG AGCAGGGAGG GCCGTGTGGA CACTTAGCTC 1080
CTCTGTCTGC AGGTTGTACA ACTTCAATCG TCCGGCAGGC CCGTGAGCAC CTTCGGTGTG 1140
ACAGTCTGTT CAGCACTGGG GCTATAAAGA TAAACAAGAC AAAGTCCATG TGCTCAAAGA 1200
GCTCTCCGTC TGTGATCCCA GAGAGACATC TGGACAGAGA CGTCAAAATA CAAAACAATA 1260
AATTCTGGAC AGAGCAGTGT TTAGCATGAA TCGTGATCTG GAGGACAAAG ACACAGTCCT 1320
TGCTGTCACG GAGCTCACCA TTGAGGGATG CCCACAGGCA GCTGAAATAC AGCGGAAGTG 1380
ATAAATCTTT AACAGAGGGT GTTTTACTCG GGGCACCCAG AAAAAAATGA AATTTTAACT 1440
GCAGATTCAG GAAGTTATCC ATGAAAAGGC GGCAGTTGAT TCCAAACTCC AACAATGCGC 1500
TGTCAAGGCT CATGGGCTGG CTGAGACCGT CACTTCAGGC AGAGGATGTA GCGTTCTGAG 1560
GGGAAGAAAA AGTTTTAAAA AGAAACTTCC AGAGACACTG TCTTGATGCA AGGAGTAAAC 1620
ATAAAGTACA AATCTGGAAC ACAGCGTCAG ACTTATTAGG AAAGTTACTC GGATCAGGGC 1680
CTCTGAAATC ACCCAGACCC GAGCTCCGTA ACTGCTCTGG TATAGAGCTG GGCTCTGTGC 1740
TATGGAGACA 1750