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

TagContent
EnhancerAtlas ID
HS003-32417 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr3:50285600-50287250 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2298952chr350286953hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EsrrgMA0643.1chr3:50286133-50286143ATGACCTTGA-6.02
IRF1MA0050.2chr3:50286228-50286249GAGGGGAAAATGAAACTTGAA-6.21
RORAMA0071.1chr3:50286134-50286144TGACCTTGAT-6.02
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_00328chr3:50272275-50294504Adipose_Nuclei
SE_00924chr3:50285666-50287046Adrenal_Gland
SE_01672chr3:50284685-50287092Aorta
SE_02846chr3:50285577-50286779Astrocytes
SE_03917chr3:50285788-50288246Brain_Anterior_Caudate
SE_04864chr3:50278146-50288370Brain_Cingulate_Gyrus
SE_05809chr3:50271925-50313735Brain_Hippocampus_Middle
SE_06748chr3:50285481-50287184Brain_Hippocampus_Middle_150
SE_07819chr3:50273449-50289446Brain_Inferior_Temporal_Lobe
SE_09475chr3:50273514-50296642CD14
SE_13800chr3:50285674-50287008CD34_Primary_RO01536
SE_17710chr3:50272093-50288404CD4p_CD25-_CD45RAp_Naive
SE_18113chr3:50272067-50287604CD4p_CD25-_CD45ROp_Memory
SE_18975chr3:50273503-50289925CD4p_CD25-_Il17-_PMAstim_Th
SE_19368chr3:50281643-50288383CD4p_CD25-_Il17p_PMAstim_Th17
SE_22929chr3:50281635-50287445CD8_primiary
SE_23202chr3:50285581-50286986Colon_Crypt_1
SE_23879chr3:50285586-50286178Colon_Crypt_2
SE_23879chr3:50286180-50286903Colon_Crypt_2
SE_24968chr3:50285688-50286873Colon_Crypt_3
SE_26040chr3:50285735-50287016Duodenum_Smooth_Muscle
SE_26665chr3:50285511-50290083Esophagus
SE_29626chr3:50285527-50287062Fetal_Muscle
SE_31450chr3:50285500-50288273Gastric
SE_34350chr3:50281572-50287028HCT-116
SE_34830chr3:50282763-50288102HeLa
SE_36596chr3:50282561-50287261HMEC
SE_38192chr3:50273512-50288122HUVEC
SE_40718chr3:50282578-50288388Left_Ventricle
SE_42127chr3:50271906-50288361Lung
SE_45312chr3:50285574-50286771NHLF
SE_48477chr3:50282625-50288375Psoas_Muscle
SE_48622chr3:50282644-50288331Right_Atrium
SE_49541chr3:50285655-50286831Right_Ventricle
SE_50198chr3:50282598-50288279Sigmoid_Colon
SE_52519chr3:50282642-50288279Small_Intestine
SE_53321chr3:50271955-50288381Spleen
SE_57397chr3:50286092-50286932VACO_503
SE_62832chr3:50263305-50298785Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr35028577750286185
Enhancer Sequence
GGTTGAACCG GGAGGCAAAG GTTGCAGTGA GCCAAGATCA TGCTATTGCA CTCCAGCCTG 60
AGCAACAGAG CGAGACTGTG TTTCAAAAAA AAAATCTGGA CTCAGCCACC CCTCTGAGAG 120
GCAGGTGCGA GGGGAGCTGG GTGTGTGCAA AACTCACAGA TAAGCCTCTT GCCAGCTTAT 180
CTGGTAGGGG GCATCCCTCA GGTCCTGATG GAAAGAGGAC CCAGCCAGAG ATGGGGAGAG 240
TGAAGCTACT ACCCCACAGC TGCCAGGGCA CTTAGCCTGT GGGCTGCCCG AGAGCTCTTC 300
ACCCCACCCA TTCCACCCAG ATGCCATCCT GGGGCTCCAC CCACCTCTGC TCCTGTCCCC 360
CTTCTCTGCT GGAGCTGCTC CTGGGCTGTG CCCCTGCCTC TGTCCCGTTG TTCCCCCTGC 420
TTCCTGCCTG GCTGCCAGCA CCACACCCTT GTCCTGCCAC TCACTACTTC CCGCCTGAGT 480
CACAGCTGCT GGAAAGACAA AGAGACCAGC CTGAGTCTAG GGATAGGGGC TCCATGACCT 540
TGATTTGCTT ACCTGTCAAG TGGAACTCTT TTTTCAGTGA CCCCTGCTTG GGATAGAGAA 600
TGTTCTCTTA ACATTTAAGA GGCCTTAGGA GGGGAAAATG AAACTTGAAG GGGACAGGGA 660
AGTGGGCCCT CCCTGGCTGG GGCAGGGAGC AGATATCCTG GCTCCTAGTG TGACTGGCTC 720
TGTGCTGCCT ACCTCATGTC TACCAGGTCT AGCTGCTGCT AGGAAAATCA GATGCAAAGC 780
AAGTTTGCAC CCTCGTCCCT GGGCAGGGTC ACGAAGCGGC CCACATCACC TACTAAGAGT 840
GGGCAAAAGG CCAGACCCCC TCTTCACTCT CAGTGGCCAG ATAGGGAAAC TGATGCCTCA 900
AGTGGGCAGG AGTCCCGAAG TCACACAAGA TGGGGAAGCT TTCACCCTAG ACCTCAGGTC 960
CCCCATGCCC TGGGTAGCTT CCCTGCTGAG TCTGAGCTCG CCTGGCTCGG GACTGCATGG 1020
GGACCCATGA CTTCGCATCC TTGGCCTCTG CTCCTGCAGT TCCCCCCATC CTGGCTGTGA 1080
CTGGCTCCTG GTTCTTCCTC CTGCTCTGGA GGAGCCAGTG GGGAAGACAG TCAGGTAGCC 1140
ACTGCTGCCC TCCCTGCCCC AGTGGGTGCT TTGAGCCCCA GGGGGATGGG CCTTAAGTGT 1200
TCAGGCATCG CTGTGAGGCT TTCCTGGGAC CTTTCCCCAT GTCCTCATTG GCAGGTGGAG 1260
GAGTGTTGGT ATGCAGATCC TGGCTGCCCC TTTGCCATGC ACAGCCCAAT GGGGAGGGAG 1320
TGGTGCTGGT ATATATCCCG GTACACACCC CAGTGAAGAT ACTGGGCCCG GCCCCTGTAG 1380
TGCCCAGGGG CTAAAGCAAT AGAGGGGATT GCTGCCCCAG CCACAGCGCC CCAGCCTTCC 1440
CAGGGCCTGC ACATTTGTAT GTCCACAAGA TTGTGCAACC ATCACTGCTA TCTAATTCCA 1500
GAACATAATC ACCACCCTCA AAAATAAACT TCATACCCAA CTAGCTGTCA CTCCCCATCT 1560
CCCCAGATCC CCTCCCCTCA TCCTGGAAAG CAGGCCTGGG ACAGTCAGAA GCTCAGTGAT 1620
TGCAGGCGCC TGATGGCATT TGTGAGGAGG 1650