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

TagContent
EnhancerAtlas ID
HS073-07490 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr19:18588710-18591410 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11670056chr1918589943hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr19:18588962-18588973CCACACCCTCT+6.02
Nr2f6(var.2)MA0728.1chr19:18590302-18590317GAGGTCAGGAGTTCA+6.22
SOX10MA0442.2chr19:18591169-18591180AAAACAAAGGA+6.32
Sox3MA0514.1chr19:18591169-18591179AAAACAAAGG-6.02
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_01013chr19:18588643-18590394Adrenal_Gland
SE_01013chr19:18590470-18592196Adrenal_Gland
SE_04099chr19:18588738-18590106Brain_Anterior_Caudate
SE_04099chr19:18590344-18591643Brain_Anterior_Caudate
SE_06012chr19:18587569-18592062Brain_Hippocampus_Middle
SE_08139chr19:18590405-18591646Brain_Inferior_Temporal_Lobe
SE_09318chr19:18587289-18593113CD14
SE_12155chr19:18588799-18590417CD3
SE_12155chr19:18590474-18591063CD3
SE_15037chr19:18589123-18590617CD4_Memory_Primary_7pool
SE_17983chr19:18583928-18591813CD4p_CD25-_CD45ROp_Memory
SE_19379chr19:18587487-18590403CD4p_CD25-_Il17p_PMAstim_Th17
SE_19379chr19:18590449-18593306CD4p_CD25-_Il17p_PMAstim_Th17
SE_20439chr19:18584612-18591598CD56
SE_21047chr19:18588603-18591663CD8_Memory_7pool
SE_22689chr19:18583973-18591671CD8_primiary
SE_23216chr19:18590556-18591559Colon_Crypt_1
SE_23893chr19:18589312-18590189Colon_Crypt_2
SE_23893chr19:18590542-18590954Colon_Crypt_2
SE_23893chr19:18591073-18591477Colon_Crypt_2
SE_26168chr19:18588425-18592741Duodenum_Smooth_Muscle
SE_26932chr19:18588122-18592042Esophagus
SE_31681chr19:18588601-18590332Gastric
SE_31681chr19:18590369-18592244Gastric
SE_41123chr19:18587807-18590387Left_Ventricle
SE_41123chr19:18590510-18591609Left_Ventricle
SE_41560chr19:18589244-18590155LNCaP
SE_41560chr19:18590567-18591450LNCaP
SE_42344chr19:18587292-18590373Lung
SE_42344chr19:18590412-18592352Lung
SE_44495chr19:18587274-18592340NHDF-Ad
SE_46271chr19:18587413-18593123Osteoblasts
SE_47511chr19:18588888-18589813Pancreas
SE_47511chr19:18589872-18590274Pancreas
SE_47511chr19:18590495-18591608Pancreas
SE_48120chr19:18587362-18592202Psoas_Muscle
SE_48694chr19:18588545-18590349Right_Atrium
SE_48694chr19:18590432-18591600Right_Atrium
SE_50125chr19:18585873-18593035Sigmoid_Colon
SE_51145chr19:18587336-18592595Skeletal_Muscle
SE_52434chr19:18585882-18592848Small_Intestine
SE_53541chr19:18587934-18592552Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr191859051618590939
chr191858971418590055
chr191858920018589384
Number: 1             
IDChromosomeStartEnd
GH19I018472chr191858378718592442
Enhancer Sequence
AGTGAGGCTG GGGTTTTGAA TGTGGGGTGC TAAATAGATG GTGATGAGAA CACAAGGACT 60
GGGTGGGGGG GATGAGAAAA AACACAGAAA GCAGCTGGGG TGCAGTGCCC TGACAAGCCA 120
ATCAAGGGCC CAGGAGGTGA GTGTCGGCTG CAGACAGGCA GAGCCAGCTA GGTCCCTTCA 180
CGGTGGGACC AGCTGTCACC CTCTGTGCTC ACCAGCCTGG CCTGGTGGGG ACGCCTGACA 240
GCATGTGGCC CACCACACCC TCTTCTGGCT GCTCCCTCCA GAGCCAACAT GCGTGGTGTC 300
ATGGCCGAAC CCTTGTCAGG GGGGCCAAGC GCCTCGTTAC CTCATCTATG AAGCAGGACA 360
GAGGGTCAGG AACAGACTGT AGCACAGGTG ATTTCCCTGC TGCCTTAGAA GCTTTGGGGT 420
TGGCCTCAGG CTGCATTAAT TAAATAACGG GGTAACTCAG TAGCACATGA CACCTGCAGG 480
GTACTGCCCA TCTCACACCC AAGAACACCC AGCAGGGGAG AGCCATGCCT CAGGCCACCG 540
CCTGCCCAGT CTCTGTAGAC CCTCTGAGGG GTCATCACCC CCACAAGTCC TCTCAGGCCC 600
TCGAGTGGCA AAAATCCAAC TTTCATTACC CAGCATGAGG TATGGAACTG GGAGCTCCTG 660
AGATACAAAG TCACCCCCGC TGCTGTACTT CAGGCCAGGG CCCCAGGTGG GAGCTGGGGA 720
GCCTGGTAGG GCCGCCACAG CTGGCCTGAC ACAGTCAGCA GGTCAGCTGG GTCTTCAAGG 780
CCGGACAGGC AGGCACTGAG CTGTGCCGAG GCTGGTGCTC CCCAGACCCA ACTGGACTTC 840
AGACCCTGAC TCGGAGAACA GACCTCAACA CAGCAGGGCA GTGATGCCTG CGCCCTGCGG 900
TCACTTGGCC TGGGCGCCCA CTGGGGCTAC TGAACACAGA CTGGGAGACT CCTGTAGGCA 960
GCTCCCCCTC AATGAGGACA CTCCTGTAAA GACAGCAATG CCTTTGGGAA AAGGGTCGAG 1020
GGTGCAGAGC CTGGGAGGCA GTGAGAGTCC TCAATGCTGA GACAGAGGAA AGGGTGAGGA 1080
GGAACCTCTC CAGGGCCAGA ATCCCCTGAT CCTCTCCCCT CCGGCAAAGA GCACTTCCGG 1140
GGATGAAGCA ACAGGAAGTG GCTTACGAAA TCCACCTCCA GGCCGAGTGA CCAGTTTACA 1200
GGAAGTGTGG TGGGTGAATC TTCCCCAGGG CACGAGGCAA TGTCTGGAGC CATTTCTGGT 1260
CCTCACCACT GAGGGCGGGG ACAGTCCCCA CCATCTGGCT CGGGGGAGGC CAGGGATGCT 1320
GCTCAGCACA CTGCAGGCAA CACAGAACCT CCTGCCCCAA ATGTCAAGCA GTGCAGGGGC 1380
TGAGAAGCCC TGGGCTGACC CTGCCACGGG AAGCGACCAT CAGAGCAGAA AGCAGAAAAA 1440
TCTATGGGAA AAAAGACCTG CTCCCTTCAA CAAATATAAA ATATAAATGG AAAAGTTACG 1500
GGTGAAGAAG AACGTATCTG ATTGTTGGCC AGGCATGGTA CCTCACACCT GTAATCCCAG 1560
CATTTTGGGA GGCTGAGGCA GGTGGACTGC TTGAGGTCAG GAGTTCAAGA CCAGCCTGAC 1620
CAACATGGTG AAACTCCATC TCTACTAAAA ATACAAAAAT TAGCCAGGCA TGGTGGCATA 1680
CGCCTATAAT CCTAGCTACT CGGGAGCCTG AGGCAGGAGA ACTGCTTGAA CCCGGTAGGC 1740
GGAGGTTGCA GTGAGCTGAG ATCAAGCCAC TGCACTCCAG CCTGCACGAC AGAGTGAGAC 1800
TCCATCTCAA AAAAAAAAAA AAAAAAAAAT CTAGGATTGT TTTAAAAACT CTCCAGCAAA 1860
GACAGAAACT AGGGAGAGGG CACAGTGAAG AGATGAGACA CACAGACAGA TGGACGGGGC 1920
CCAATCTGGC CAGGTCCCAG GATACCTGCT ACCAGCCTGG GGACAATGAG GCCCAAGGCA 1980
GCAGGTGCCA AGGCTGCCCC AAAGACACAT GATCCTTCCC ACCACCCTCC AGAAGCACCC 2040
ACTCAGCAGA AGTGCCCACT CTCCCCAGGC AGCACGTTCT CCCTGCTGTC TACTGGGCAA 2100
GGCCTGCCAC CCCACCCCTG ATGCAGGAAA TGACAGAAAG GAATGCATCT GTTCCTTCTT 2160
CAGAAGTCCA TCTTGCTGAC TCTCCCAAGC ACCAGTGTCA GCACACACGT CCTGATCTTA 2220
CAGAGCTGGG TCACCCTGCC AAGCCACGGC GTGTGGTCCA GCAGAGGGAA GGTGAAGTCC 2280
CGGGAAGAGC CCTGGACGGT GGCCTCCCCA CAACAGGCCC CCCCTTTCCA GTAAAGCACA 2340
AATGATTGGG AAACGCTATT CAGGAATCCT CCTTGAGACT TCCTGGCAGG ACTGGAGCAG 2400
GACATTGAGG CCACGGAGAG TTTAGACAGT GACTGAGTGG GGCTGTCTCC GTGAACTACA 2460
AAACAAAGGA AGATCTGCCC AGTGAGCTTG GTTGGCTCAG GGACGAGCTA GGGAACTTGG 2520
ACAGACACAT TGTGGACCTC ACTGGTTCCA GCCTAGGGAA CCAGGTGGCC ACGGTCAGGG 2580
CAGAGCAGAG GGCAGGACCC ACGGCAGCTC CTCTGCCAGC CTGGGAGGAC AGATGGTGTG 2640
TTCAGCAGGC CAGGTGGGCC TGTAAGAGCA GGAAAGGGAC TCCAACTGGC TACAAGCCAA 2700