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

TagContent
EnhancerAtlas ID
HS050-01019 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:21633190-21638000 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs74698898chr121633211hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr1:21636265-21636286TTTTTCTTTCTTTTTTTTTTT+6.59
NFYAMA0060.3chr1:21636885-21636896TCTGATTGGCC-6.02
ZfxMA0146.2chr1:21636531-21636545CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00105chr1:21636649-21638133Adipose_Nuclei
SE_00854chr1:21633214-21636405Adrenal_Gland
SE_00854chr1:21636483-21637891Adrenal_Gland
SE_01643chr1:21634033-21636272Aorta
SE_03598chr1:21636787-21637696Brain_Angular_Gyrus
SE_04518chr1:21636410-21637988Brain_Anterior_Caudate
SE_05710chr1:21634990-21636313Brain_Cingulate_Gyrus
SE_05710chr1:21636462-21638087Brain_Cingulate_Gyrus
SE_05944chr1:21633077-21638154Brain_Hippocampus_Middle
SE_08398chr1:21633501-21638178Brain_Inferior_Temporal_Lobe
SE_12161chr1:21633335-21634139CD3
SE_15142chr1:21635160-21636148CD4_Memory_Primary_7pool
SE_17692chr1:21633251-21634336CD4p_CD25-_CD45RAp_Naive
SE_18622chr1:21634330-21635856CD4p_CD25-_Il17-_PMAstim_Th
SE_26127chr1:21635142-21636299Duodenum_Smooth_Muscle
SE_26770chr1:21634339-21636405Esophagus
SE_26770chr1:21636649-21637696Esophagus
SE_31433chr1:21634419-21636259Gastric
SE_31433chr1:21636476-21638003Gastric
SE_46660chr1:21634561-21635094Ovary
SE_46660chr1:21635700-21636230Ovary
SE_48583chr1:21634013-21636131Right_Atrium
SE_54639chr1:21630709-21637916Stomach_Smooth_Muscle
SE_56171chr1:21633655-21634878u87
SE_56171chr1:21635019-21636213u87
SE_65263chr1:21633994-21636234Pancreatic_islets
SE_67931chr1:21633655-21634878u87
SE_67931chr1:21635019-21636213u87
SE_68932chr1:21633171-21636100H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr12163443821634710
chr12163530421636088
chr12163650721637106
chr12163661121637909
Number: 4             
IDChromosomeStartEnd
GH01I021306chr12163333621634139
GH01I021307chr12163429421636187
GH01I021310chr12163654121637410
GH01I021311chr12163762121637770
Enhancer Sequence
CAGCTCTAAG GCATTTGGGA TCTGAACCCA GGCAATATGA CTCCAACTTG ACCCTAACCA 60
GTACAGTGAT GGCCTCACTG CAGAGAGCGA TGAGTGTTAC AAAGACAGGG CAGCAGCGAG 120
GTGTGCTCAA GCCTCTGGGG AGGAGTCGAG GAAGGTCTCC ATGAGCCCTG TCTGACCAAC 180
CCCCCCAATC TACAGATGAA CTAACTGAGG CCCCCTGGAC ATGCTGAGTC AGGGACACAG 240
TCAGGACTAG AAGCCAGGCT TTTATACTCC CGGCCCAGTG CTCCTTCCAA AGCCCTGCAA 300
CTGTGCCACA AATGCTAAGG GCCTGGCAGC GAGGACTGAG CCAACTCTTG GGCTTAGGAT 360
GACTGAGGTC CACCGAGGAC TCCCTCGTCT CCCTGCACTC AAGACTCTCC CCTTCCTCTG 420
GGTCCAGCAT GGGTCTCAGC TCCCAGACTG CTCCCTGCTT AGAACTCCTG TCCACATTAC 480
CCCAGCCCGG GCCCTGTAAT GCTGGCTTTA ACATTTCCAA AGCGGGCTCG TTCCCTTTAA 540
TTCACTTTTG CTCTTCACAG CGACTCTGGG GGGCTGGAGC TAGCATCTCC ACATCATGGG 600
TGGAAGATAG ATCTCAAGGT CAGACACATT TGGCTGCTTA GCAGCTGTGT GATGTTGAGC 660
GAGTCATGTC ACCTCTCGGA GCCTCAATTT CCTCCCTCTG CATGGTGAGG GTGGCAGTGG 720
CTTCCTTGCC GGGGGTTATG AGCATCTAGT GAGACACCAC TAGAGTCTGT GTAAAGTGCC 780
AAGCACAGTG GCTGGCACAT ATTAAGTATT TCATAAAAAG CAAGTTTTAA ACATGATCAC 840
TACAGTCATT GATGTGAGGA CGTCAGCAGC AGAGGGGCCT CCAGAGGACA TTTTCTTGCA 900
CCCCAGGAGG CATTCCTGTC ATTTGTCCCC ACTGGGTCTG GGGCTGGGGC TTCTTTGTAC 960
CTCTGAGGTA CAAAGTGGAA GCTCTGCCTG GCTGGCAAGA CCAGACCTGT TGTGGCGGCC 1020
AGGCTGTACC CACGCAGGGC CACTGCTCCT AGGGCACTGG GCTCCAGACA GAAAATGGGA 1080
AGGGACAGAT AAGCCTCTAT GAAAGGTGGC CAGGCACAGG AAAGAGGCCC TGCCCCCTTG 1140
AGAGGGAGGC CCTGCCCCCT TGAGAGGTTG GCCCCGCCTT GAGCATCCTT GTCAGGCAGA 1200
GATCTGGGCA GGACAGAAGA GAGGAGGTGC CTGGCTCAGT TTTGCTGCGA TCCCAATGGG 1260
TCACACGCCT TCTGGATCCC CCCAGAAGGT CTAGAATGGG GTCACCCCTC AAAACCTCCC 1320
TGGCTCACTC TTAGCTTGGA ACCATGAACG AGCTTGCTCC CACCCACATG GAAAGCAGCT 1380
GCCCTTCCCC TGGAGACATT TTCCACTTCT CTACCTCCAG ACCTCTGCTC ATGCTGTTTC 1440
CTCCACCTGG TAAACCTCAC TCTCTGCTGT GCTGTCAGAA AATGGCCAAC CTTTTGAGTC 1500
TCAGCTGAAA TGGCACTCCC TTTGCCCCAG CTTTAGTTTA ACAAGCATTT GTGCATGCTC 1560
TGGAGATGGG CTGTCCTGCC CTCATACACC CTGCTAGGGC CTAGCCAATG AGGGACAACC 1620
GGAAGTCTTA CCCTCCAGCC CCCACCCCGG AGACCACCTG TGTAGGACCC CCAGGGGTTG 1680
CCAGGATCCT CCCCACAAAC GGCAAAGCAC TCTCTATTTG GGGGAACAGC CCTTCTCTGG 1740
AATTGGGAGT AACAAGAGGA AGGGAGGAAG GGCGTCTTGT GAGAGGGAGG GGCCAGGAGG 1800
CCTGAGGGAG CTCTGGCGTG TGTTCCAGAA ACCCTTTGGG ATCAGAGACA AGATCAAAGA 1860
GGCAGCCTTC ATGAGGCTGT CCAGGGCCCT GGACATGGAC CCAGGAAAAT TGGCTGGGTG 1920
ACCTCAAGCA AGTTACTTGC CCTTGCTGAG CCTCAACCTC CTCATTTGTG AAACAGGGCT 1980
AGTACCCCCA ACCTCTGAAT GAGACGGTGA ACAGCCTTTG TGCATGGGAG GGGCTTGAGT 2040
CTGGGTACTG AGGGGCGAGC TGGGGCCTGA GCGAATGCTG CAAGTCCCCC AGGGCTCCTT 2100
CTCTGATGCC GTGTCTCAGA GCCCCCTCCC CTTCCTGCCT GCCCAGGGTT TCCCTTGCTA 2160
GGAGCAGTTT TAAAACTCCC CAGTACCTGG GCTATGAGCC ACAGCTTCTT AAAGTTCCCC 2220
ATCTCCTGCA GCAGGCTTAG TTGGACTGAG CCAGAGCCCA TCATTCACTG TTTCTGGAGA 2280
TTATCACAGT TTGCAGAAAC AGCAGGGCAC CTAGCAGGAA TCTGGCACAG GCTCCTCGCT 2340
AGTTGGGACT GGAACTGGGC CAGGACAGCA CCTCGTGTCC TCTAAAAGGA TCCACAGGGC 2400
CTTCCCTCTC TCCTTTCCCC TCACTCAGGC ACACTGGGGT TCCAGAGTTC TAGGGCCACA 2460
TCCCAGACAC AGGCACTGCA GTCTTGTCCC CACTGGGATA TGAGACACAG AAAGAACCCT 2520
GGGCTGGAGT CAGGGGAGGA TGGTCACTCC CCCTCTGTGG TTAAGGACAG AAACTCTGGA 2580
GCCAGACTGC TGGCGTTCAA ACCCTGGCTC TGTCATTTAC CAACTGTGAC CTTGAGTGAG 2640
TTACTTAACC TCTCTGTGCC TCTGTCTTCT CACCTGTAAA GTGGTGAATC ACAGTACCCG 2700
TCCCACCAAG TTGTTGGGAG GATGCAGTTA GTTACCCAGA AAGTGTTTGG AGTAGTGCCT 2760
GGTATGCAGT GAGCGCTGGC TTGGTTGGGT GAATGAATGG GTGCATGAAG GAATGAGTCA 2820
ATGCGTCGGA GCTCTGCTCT GTGGCACGAG GCCCTTCAGG ATCTGCCCGG ACATCAGCAC 2880
CTGCCATTGT CCCAAGCAGG TCATGATCAC ATCCTTCCCA CCAGCTTCCT TGGCTTGGCA 2940
TAACCTCACC ATTGCTGTTA GTCCCAAGAA CTCCTTCAAC ACATGCTTCA AATGCCACCT 3000
CCTCTCTGAA GCCTCTTCAA TCAGGACCCT CAGGGCTGTT AATGATAAAA ACCAAACCCA 3060
GCTGGATTTT CTTTTTTTTT CTTTCTTTTT TTTTTTTTTT TTGAGACGTT TTGAGACGGA 3120
GTCTCGCTCT GTCGCCCAGG CTAGAGTGTA GTGGCGCGAT CTCGGCTCAC TGCAAGCTCC 3180
GCCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCG AGTAGGTGGG ACTACAGGCG 3240
CCCGCCACCA CACCCGGCTA TTTCTTGTAT TTTTAGTAGA GACGGGGTTT CACCGTGTTA 3300
GCCAGGATGG TCTCGATCTC CTGACCTCGT GTCGTGATCC ACCCGCCTCG GCCTCCCAAA 3360
GTGCTGGGAT TACAGGCGTG AGCCACTGTG CCAGGCCCCA GCTGGATTTT CTAACAAAAC 3420
AAACATCTTG GCTCACATTG CCTCAGAGGG AGGGAGGGAG GATCATCAGG CAGGAGACGA 3480
TCCAGGAGTT CAGATGCTGC TGCTAGATTT CTCTCCCCTG CCTCATCTTC CATGCCTCAT 3540
CTTCCCCTTG TGTGTTACCT TCACTCTCAT CTCTGAGATT AGACATCCTT CACACCCAGA 3600
GAATTCGGCC AGGCTTACCT TGTGGTAGCT GAGAGCCCTA GAGAAAAAAA ACCTTCTCTC 3660
TCCCTGGGCT GAATTAGAAA GTCCCAGGGA AGAACTCTGA TTGGCCAGGC CTGTTTCCTG 3720
TGCCCTCCCC TGTGACTTAG TAGAGGTGGG GCCTGATGCT GTGATTGACA GCCTGGTTAA 3780
TCGGCTAAAC TCAGTAGGCG TGTCCCATGC ACCACAAGGA ATTGGGGAGG AACAATTCCC 3840
AAAGGAAGGA GGTTGCTGTT AGCAGAAGAA AGGCAAAACA ACCTGTGTCC ACATCATCCC 3900
TCCTGCCACC TCTGGCCCTG TGCTTTCACT GCACTCTGCA CACACCCCCA GCAGACCCCA 3960
CCCGAGCTTC CAGGGATGAT TTGGGTACTT GGGTATGGGT GACTGTCCCT GCCACTGGAC 4020
GATGAAGTCT TAAAGGGCCA AGACTCTGGT CACCTTGGCT CTCCCAGCCC TCTGCTCTGT 4080
CCCTGATCAT AAACTACTTT TGACGAACGA AGAAAACGAA GGATCAAGGA ATAGAAGGGG 4140
TTGTGTAAGG GGCCAACCAG GATGAAAATC TTCATCTAGG CTCTTCCAAC CCTACCCTGC 4200
AGCCTCCTCC CTCAACCCAC AATCAGCAAC ATATCCTACA AAAACATGTT GACAAGGAAA 4260
CCATCACCCA CCCCTCAGGA GGCAAGAGAT GGCCCCAGCT CAGTGCCCCT GTGAGGAAAG 4320
CTGGACCTAC ATTCAAAACC AGCTTCTGTC AAAGACACAT TCTGCCATCG TGGGCAATCA 4380
GGCTGGTAGT GAGGATGAAA TGAGAGAATG TAGACAAAGT GTGTGGCACA CAATAGGGAC 4440
TTGATGAATG GGGGCTGTTG TTTTCAGAGT GGGGCTCCCT GGCCAGCTCA GGGCCATGGC 4500
TGGGTCTGGC TGGCTGCCCA CACCACAGGG CCTGCAGGGT CACACCCCCA GTGCCTCCCT 4560
TTTGTTGCCC AACATGCAGG AATGTTCATA GCATCTGTGC CCTCCTCTGT CCACCCATTT 4620
ATAAACTCAG TAGGCGTGTC CCATGCACCA CCAACAGCGC AGGCTTCCAG GGCAAGTGAG 4680
AAAAGAGCAT GCGGGCCGGG CATGGGGGTT CACGCCTGTG ATCCCAGCAC TTTGGGAGGC 4740
TGAGGCAGGA GGATCGCTTG AGACCAGCAG TTTGAGACCA GCCTGGGGAA CATAGTGAGA 4800
CCCTGTCTCC 4810