EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-33338 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr19:18616720-18619200 
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_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_23893chr19:18613414-18617350Colon_Crypt_2
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: 3             
ChromosomeStartEnd
chr191861744918618539
chr191861840018618511
chr191861690718617225
Number: 1             
IDChromosomeStartEnd
GH19I018498chr191860923418621009
Enhancer Sequence
CCACTGTACA GTCAGGTACC CCCACCCTGT GTCCTGCTCT GTACTACACA GACCACCCAG 60
CACACATGTG GCCAATACCA GTGAGGCAAA GGTGGCAGCC TGGGCCCCCC ATGCTGGCCC 120
TCAGCCATCC CTGGGACAAC AGTCTAGACA CCCAGAAGCT CTGCACCTAG GCCCACTGAC 180
CCAGCCTCCC TCCAAGCCCT GGGTGCCCAT GTGTGCCCAG GCTGCTGCCC CTGGCACTCA 240
GGCCATGCCA CACGCAGCAG CTGGGTCTGA AGCCTGGCTT GGAACCAGCC CCCCACAGTC 300
AACATGGAGA CAGCCCTGCT GGCACCGCCC CAGGCCTGGG CCCTGTCTCC CGCACCCTCC 360
AGCGACCTGC CTGGGCCACC CTCAAGGTGC GCCTGCTCCT AAGCCGCCTC CCACAGTGGA 420
GGGACACCCG GGCTGCTTCA GAGCAGACTG TGGCAAGTTA CCCTCTCCCC CAGGGGGAAA 480
GGGATCCAAA GCTCCTGTGC CTCTGGGGTG CAGCATCAGC CCAGACTTCT GCTCGGCTGG 540
GTGCCATGGC TCACGCCTGT AAGCCCAGCA CATTGGGAGG CCAAGGCAGG AAGTTCGTTT 600
GAGGTCAGGG GTTTGAGACC AGGCTGAGCA ACACAGGGAG ACTCTGTCTC CATATAAATA 660
AAAAATTAGC CAGGTGTGGT GCCACGCACT TGTAGTCCCA GCTATTTGGG AGGCTGAGGT 720
AGGAGGATCA CTTGAGCCCG GGAGCCAAGG CTGCAGTGAG CTATGATCAC ACCACTGCAC 780
CCCAGCCTGG ATGACAGAGC AAGACCTCGT CTGAAAAAAC AAAAGCAGAC TTCCGTTCAA 840
CAGCATGTGA ACCTCACCTT GCACACCTAG GAGTTCGTTA CCCTCCTCAG CTCAGAGATT 900
AGAGGGAACT CTCCCCACAG AGATGCTATG ATCAGAGGGC CAGGGACCCT GTCTCATTGA 960
TCCTACGCTC TACGCCAGAC ATCGCCTCAG AATCCTTCTC AACACGGCTC CACTTCCTAT 1020
CTACAAGGAG CTGGCCTACA AGATGGAAGC GATTCCTACA TTATGGGGTC ATGTGGCTCC 1080
AGGCACATGG CCCTCGACCA GTGGGAGCCT GTGCACAGGT AAGAGAGCCA GGGCAGCCTG 1140
GAGATGAGCT GGACACAGGC TGCCAGCACT GGCTGTCCCC TCCCACTTGC CAAATCCAGT 1200
GTGAGCTGAG CACATTTCAC TGGAACAAGC AGGCGTCTGA GAGCATCCAA CTCCAAAAAT 1260
AGTGCCACCA GGAGAGGAAG GAACACGCTC TTCTAGCTGC ACCCGCTCCC TGCCCTCAGA 1320
TACCTCCCTG CACAGTCTGT GCCTGGCCTG TGGCAGTTCA AGGGTCACAC CCAACTCTGA 1380
AAAGGGAGAG ATAACATCCC CAGATAAGAA GAGTGAAAAC AGGCCAAGTC TGCTGCCAGA 1440
GCCTGGCCAC AGACCCACAG CCCCTTGGCA GAGAACTGCT CAGGAAGTCC TCCTCTGAGT 1500
CTTTCAAGCC ACTGGTATCT AACAAAGAAT CTAATCTGCA CACGGCACTT GCCCCGAGCT 1560
AAGAAAGTTC TGGAAGGGTC TCCTAGGTCT CCCCAGCCCA AGGTGAGCTT GCTTCTGTGG 1620
AGGGAGATGC CTGCCTGCCC ATGTCCACCA CCACTGCACA CCAAGCCAGT CTGAAGCCAC 1680
CATGATCTGG CTGTTGCTGG TTTATGGTGC ACCTCCCCGC TGCGAAGAAG TGGGCCATGT 1740
GAGCGCAGGG GCTTCATCCC TCCTGCTTCT TACTGGAGAA ACACTCCTGG AGGCAGCCGA 1800
ACCCTCACTG GGTGCAATCC CTCTGTGTAG GAGATTGCAC TGTGTAGGTT GTGCCCCGCC 1860
GAACAACCAC GCAGCTGAGG CTCAGCTCAG AGACTGCATT CAGAGCCCAA CTAGAATCAG 1920
ACACAGGTTC TGCGGGCCCC ACTACCCATC TGGAGGCAGA CGCCTGACCC CCAGCTCCAT 1980
CCCCAGAGAT GAGGATGCAG CAGGCTGAGG CTGACTCCAT GCGGCAGCTG CTCCCAACTC 2040
CACAAGGGAC ACACAAGCCA GCCCTTCCCA TCCAGGCTGC ACATGACTGT GTTTTGTTTC 2100
AAAGGTCACA TACAGGTCAC AAATAAAGAG GCCGGTTCCC ACTGGAGGCT ATGTCAGGAT 2160
TGATGCAGTC CCTGAGAAAA ACTCCCGGAA AACCCAGGGA CTCCCATGCG GGCTGAGAAA 2220
CATTTTGAGT TTGCATGAGA TCAAAATAGG AGTCACAGCT GAGTGTGGTG GCTCACGCCT 2280
ATAGCACTTT GGGAGGCCAA GGCGGGAGGA TCACTTGAGG CCAGGAGTTA ACAGACTGCA 2340
GTGAGCTATG ATCACACCAC TCCACTCCAG CCTGGACAGC ACAGCAAGAC CCTCTCTCTA 2400
AAAAATAAAA ACAAAAATAG AATAAAATAA AATACAATAC AAGAGTCAGC AGCCAGGAGG 2460
GTAGCCTGTC CCAGAGTGGA 2480