EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-18213 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr19:18617450-18619240 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4808136chr1918618867hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HSF1MA0486.2chr19:18618282-18618295GAAAGTTCTGGAA-6.29
MEF2CMA0497.1chr19:18619127-18619142AAAACAAAAATAGAA+6.05
RARA(var.2)MA0730.1chr19:18618822-18618839AGGTCACATACAGGTCA+7.01
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_01013chr19:18616790-18618942Adrenal_Gland
SE_04099chr19:18612612-18621162Brain_Anterior_Caudate
SE_06012chr19:18609083-18619184Brain_Hippocampus_Middle
SE_08139chr19:18611825-18620707Brain_Inferior_Temporal_Lobe
SE_08861chr19:18618070-18618386Brain_Mid_Frontal_Lobe
SE_08861chr19:18618502-18618688Brain_Mid_Frontal_Lobe
SE_12155chr19:18614992-18619095CD3
SE_15037chr19:18615264-18618963CD4_Memory_Primary_7pool
SE_17983chr19:18613350-18619260CD4p_CD25-_CD45ROp_Memory
SE_19379chr19:18612797-18619131CD4p_CD25-_Il17p_PMAstim_Th17
SE_20439chr19:18615273-18618899CD56
SE_21047chr19:18616059-18618949CD8_Memory_7pool
SE_22689chr19:18615399-18619616CD8_primiary
SE_23216chr19:18612701-18620963Colon_Crypt_1
SE_23893chr19:18617508-18618912Colon_Crypt_2
SE_26932chr19:18616253-18618743Esophagus
SE_30600chr19:18617865-18619920Fetal_Muscle
SE_31681chr19:18616275-18619182Gastric
SE_41123chr19:18609803-18620443Left_Ventricle
SE_41560chr19:18615472-18620976LNCaP
SE_42344chr19:18610919-18620435Lung
SE_46271chr19:18617926-18619177Osteoblasts
SE_47511chr19:18617763-18618281Pancreas
SE_48120chr19:18610995-18621599Psoas_Muscle
SE_48694chr19:18610987-18621062Right_Atrium
SE_50125chr19:18610975-18620517Sigmoid_Colon
SE_51145chr19:18609758-18621004Skeletal_Muscle
SE_52434chr19:18610979-18621003Small_Intestine
SE_53541chr19:18617401-18619093Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191861840018618511
Number: 1             
IDChromosomeStartEnd
GH19I018498chr191860923418621009
Enhancer Sequence
CTTGAGCCCG GGAGCCAAGG CTGCAGTGAG CTATGATCAC ACCACTGCAC CCCAGCCTGG 60
ATGACAGAGC AAGACCTCGT CTGAAAAAAC AAAAGCAGAC TTCCGTTCAA CAGCATGTGA 120
ACCTCACCTT GCACACCTAG GAGTTCGTTA CCCTCCTCAG CTCAGAGATT AGAGGGAACT 180
CTCCCCACAG AGATGCTATG ATCAGAGGGC CAGGGACCCT GTCTCATTGA TCCTACGCTC 240
TACGCCAGAC ATCGCCTCAG AATCCTTCTC AACACGGCTC CACTTCCTAT CTACAAGGAG 300
CTGGCCTACA AGATGGAAGC GATTCCTACA TTATGGGGTC ATGTGGCTCC AGGCACATGG 360
CCCTCGACCA GTGGGAGCCT GTGCACAGGT AAGAGAGCCA GGGCAGCCTG GAGATGAGCT 420
GGACACAGGC TGCCAGCACT GGCTGTCCCC TCCCACTTGC CAAATCCAGT GTGAGCTGAG 480
CACATTTCAC TGGAACAAGC AGGCGTCTGA GAGCATCCAA CTCCAAAAAT AGTGCCACCA 540
GGAGAGGAAG GAACACGCTC TTCTAGCTGC ACCCGCTCCC TGCCCTCAGA TACCTCCCTG 600
CACAGTCTGT GCCTGGCCTG TGGCAGTTCA AGGGTCACAC CCAACTCTGA AAAGGGAGAG 660
ATAACATCCC CAGATAAGAA GAGTGAAAAC AGGCCAAGTC TGCTGCCAGA GCCTGGCCAC 720
AGACCCACAG CCCCTTGGCA GAGAACTGCT CAGGAAGTCC TCCTCTGAGT CTTTCAAGCC 780
ACTGGTATCT AACAAAGAAT CTAATCTGCA CACGGCACTT GCCCCGAGCT AAGAAAGTTC 840
TGGAAGGGTC TCCTAGGTCT CCCCAGCCCA AGGTGAGCTT GCTTCTGTGG AGGGAGATGC 900
CTGCCTGCCC ATGTCCACCA CCACTGCACA CCAAGCCAGT CTGAAGCCAC CATGATCTGG 960
CTGTTGCTGG TTTATGGTGC ACCTCCCCGC TGCGAAGAAG TGGGCCATGT GAGCGCAGGG 1020
GCTTCATCCC TCCTGCTTCT TACTGGAGAA ACACTCCTGG AGGCAGCCGA ACCCTCACTG 1080
GGTGCAATCC CTCTGTGTAG GAGATTGCAC TGTGTAGGTT GTGCCCCGCC GAACAACCAC 1140
GCAGCTGAGG CTCAGCTCAG AGACTGCATT CAGAGCCCAA CTAGAATCAG ACACAGGTTC 1200
TGCGGGCCCC ACTACCCATC TGGAGGCAGA CGCCTGACCC CCAGCTCCAT CCCCAGAGAT 1260
GAGGATGCAG CAGGCTGAGG CTGACTCCAT GCGGCAGCTG CTCCCAACTC CACAAGGGAC 1320
ACACAAGCCA GCCCTTCCCA TCCAGGCTGC ACATGACTGT GTTTTGTTTC AAAGGTCACA 1380
TACAGGTCAC AAATAAAGAG GCCGGTTCCC ACTGGAGGCT ATGTCAGGAT TGATGCAGTC 1440
CCTGAGAAAA ACTCCCGGAA AACCCAGGGA CTCCCATGCG GGCTGAGAAA CATTTTGAGT 1500
TTGCATGAGA TCAAAATAGG AGTCACAGCT GAGTGTGGTG GCTCACGCCT ATAGCACTTT 1560
GGGAGGCCAA GGCGGGAGGA TCACTTGAGG CCAGGAGTTA ACAGACTGCA GTGAGCTATG 1620
ATCACACCAC TCCACTCCAG CCTGGACAGC ACAGCAAGAC CCTCTCTCTA AAAAATAAAA 1680
ACAAAAATAG AATAAAATAA AATACAATAC AAGAGTCAGC AGCCAGGAGG GTAGCCTGTC 1740
CCAGAGTGGA TGCCCTCAGG TTCAAGGTTT GACATCATCT GCACTAACTG 1790