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

TagContent
EnhancerAtlas ID
HS040-25553 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr3:50285580-50287750 
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: 42             
IDCoordinateTissue/cell
SE_00328chr3:50272275-50294504Adipose_Nuclei
SE_00924chr3:50285666-50287046Adrenal_Gland
SE_01672chr3:50284685-50287092Aorta
SE_02846chr3:50285577-50286779Astrocytes
SE_03205chr3:50287240-50287890Brain_Angular_Gyrus
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_13800chr3:50287285-50288337CD34_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_36596chr3:50287320-50290098HMEC
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: 2             
ChromosomeStartEnd
chr35028577750286185
chr35028558150285690
Enhancer Sequence
TGCTTGAACC GGGAGGCAGA GGTTGAACCG GGAGGCAAAG GTTGCAGTGA GCCAAGATCA 60
TGCTATTGCA CTCCAGCCTG AGCAACAGAG CGAGACTGTG TTTCAAAAAA AAAATCTGGA 120
CTCAGCCACC CCTCTGAGAG GCAGGTGCGA GGGGAGCTGG GTGTGTGCAA AACTCACAGA 180
TAAGCCTCTT GCCAGCTTAT CTGGTAGGGG GCATCCCTCA GGTCCTGATG GAAAGAGGAC 240
CCAGCCAGAG ATGGGGAGAG TGAAGCTACT ACCCCACAGC TGCCAGGGCA CTTAGCCTGT 300
GGGCTGCCCG AGAGCTCTTC ACCCCACCCA TTCCACCCAG ATGCCATCCT GGGGCTCCAC 360
CCACCTCTGC TCCTGTCCCC CTTCTCTGCT GGAGCTGCTC CTGGGCTGTG CCCCTGCCTC 420
TGTCCCGTTG TTCCCCCTGC TTCCTGCCTG GCTGCCAGCA CCACACCCTT GTCCTGCCAC 480
TCACTACTTC CCGCCTGAGT CACAGCTGCT GGAAAGACAA AGAGACCAGC CTGAGTCTAG 540
GGATAGGGGC TCCATGACCT TGATTTGCTT ACCTGTCAAG TGGAACTCTT TTTTCAGTGA 600
CCCCTGCTTG GGATAGAGAA TGTTCTCTTA ACATTTAAGA GGCCTTAGGA GGGGAAAATG 660
AAACTTGAAG GGGACAGGGA AGTGGGCCCT CCCTGGCTGG GGCAGGGAGC AGATATCCTG 720
GCTCCTAGTG TGACTGGCTC TGTGCTGCCT ACCTCATGTC TACCAGGTCT AGCTGCTGCT 780
AGGAAAATCA GATGCAAAGC AAGTTTGCAC CCTCGTCCCT GGGCAGGGTC ACGAAGCGGC 840
CCACATCACC TACTAAGAGT GGGCAAAAGG CCAGACCCCC TCTTCACTCT CAGTGGCCAG 900
ATAGGGAAAC TGATGCCTCA AGTGGGCAGG AGTCCCGAAG TCACACAAGA TGGGGAAGCT 960
TTCACCCTAG ACCTCAGGTC CCCCATGCCC TGGGTAGCTT CCCTGCTGAG TCTGAGCTCG 1020
CCTGGCTCGG GACTGCATGG GGACCCATGA CTTCGCATCC TTGGCCTCTG CTCCTGCAGT 1080
TCCCCCCATC CTGGCTGTGA CTGGCTCCTG GTTCTTCCTC CTGCTCTGGA GGAGCCAGTG 1140
GGGAAGACAG TCAGGTAGCC ACTGCTGCCC TCCCTGCCCC AGTGGGTGCT TTGAGCCCCA 1200
GGGGGATGGG CCTTAAGTGT TCAGGCATCG CTGTGAGGCT TTCCTGGGAC CTTTCCCCAT 1260
GTCCTCATTG GCAGGTGGAG GAGTGTTGGT ATGCAGATCC TGGCTGCCCC TTTGCCATGC 1320
ACAGCCCAAT GGGGAGGGAG TGGTGCTGGT ATATATCCCG GTACACACCC CAGTGAAGAT 1380
ACTGGGCCCG GCCCCTGTAG TGCCCAGGGG CTAAAGCAAT AGAGGGGATT GCTGCCCCAG 1440
CCACAGCGCC CCAGCCTTCC CAGGGCCTGC ACATTTGTAT GTCCACAAGA TTGTGCAACC 1500
ATCACTGCTA TCTAATTCCA GAACATAATC ACCACCCTCA AAAATAAACT TCATACCCAA 1560
CTAGCTGTCA CTCCCCATCT CCCCAGATCC CCTCCCCTCA TCCTGGAAAG CAGGCCTGGG 1620
ACAGTCAGAA GCTCAGTGAT TGCAGGCGCC TGATGGCATT TGTGAGGAGG GCTCAGGCCT 1680
TTCCCCTCAG GGTGGTCTCT GGCGTAGGGG GCTGAAGGTG GGCAGGGGCC TTGGCAAGGC 1740
CTGCCACCAT GTCCCAATGC CTGCTGCCGC TTGTTGAGCA CTGCAGACAT GGCCCAGAGT 1800
CTGCCTGGGG AGCTAGGGAG TGAACCCAGT GCCAGGTGGA CTGTGTGGCT CCGCTGCAGT 1860
ACCAGGTACT TAGGACAGCT CTAGGAGGGA CTGCACGGTG GGCAAGTGTG CTCCCTGCAG 1920
AGGGGACTCT AACCCTGTGA CCTCAGCCTC CCTGGACCTC AGTTCCTTCA CTGGTTAGAT 1980
TGGGGTGAGA ATGGAACCTA CCTCCCAGGA TTGCTGTGGA GATGGCAGTT GGTGGGTGTC 2040
ATTGATGTAG AGCAGCATCT GGCACATGGT GGGCGCTGTT TTCATATAGC TTTGCTGTCG 2100
ATATTGCCGA TGTTATTGTT ACTGCTTGTG TTCGTTTGTG TGTTAGCACC TTCATCCTCT 2160
GAGGTTGTTT 2170