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

TagContent
EnhancerAtlas ID
HS087-00381 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr1:21633020-21637420 
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
chr12163318521633268
chr12163443821634710
chr12163530421636088
chr12163650721637106
Number: 3             
IDChromosomeStartEnd
GH01I021306chr12163333621634139
GH01I021307chr12163429421636187
GH01I021310chr12163654121637410
Enhancer Sequence
CGTTTCACCA TGTTGGCCAG GCTGTCTCGA ACTCCTGACC TCAGGTGATC TGCCCACCTC 60
GGCCTCCCAA AGTGGGATTA CAGGCCTGAG CCACTGCACC CGGCCATATT ATTGACCCTA 120
TTTTGTAGGT GAGAAAGCTG AGGCACAGAA AGGTTACAGT CAAGATCATC CAGCTCTAAG 180
GCATTTGGGA TCTGAACCCA GGCAATATGA CTCCAACTTG ACCCTAACCA GTACAGTGAT 240
GGCCTCACTG CAGAGAGCGA TGAGTGTTAC AAAGACAGGG CAGCAGCGAG GTGTGCTCAA 300
GCCTCTGGGG AGGAGTCGAG GAAGGTCTCC ATGAGCCCTG TCTGACCAAC CCCCCCAATC 360
TACAGATGAA CTAACTGAGG CCCCCTGGAC ATGCTGAGTC AGGGACACAG TCAGGACTAG 420
AAGCCAGGCT TTTATACTCC CGGCCCAGTG CTCCTTCCAA AGCCCTGCAA CTGTGCCACA 480
AATGCTAAGG GCCTGGCAGC GAGGACTGAG CCAACTCTTG GGCTTAGGAT GACTGAGGTC 540
CACCGAGGAC TCCCTCGTCT CCCTGCACTC AAGACTCTCC CCTTCCTCTG GGTCCAGCAT 600
GGGTCTCAGC TCCCAGACTG CTCCCTGCTT AGAACTCCTG TCCACATTAC CCCAGCCCGG 660
GCCCTGTAAT GCTGGCTTTA ACATTTCCAA AGCGGGCTCG TTCCCTTTAA TTCACTTTTG 720
CTCTTCACAG CGACTCTGGG GGGCTGGAGC TAGCATCTCC ACATCATGGG TGGAAGATAG 780
ATCTCAAGGT CAGACACATT TGGCTGCTTA GCAGCTGTGT GATGTTGAGC GAGTCATGTC 840
ACCTCTCGGA GCCTCAATTT CCTCCCTCTG CATGGTGAGG GTGGCAGTGG CTTCCTTGCC 900
GGGGGTTATG AGCATCTAGT GAGACACCAC TAGAGTCTGT GTAAAGTGCC AAGCACAGTG 960
GCTGGCACAT ATTAAGTATT TCATAAAAAG CAAGTTTTAA ACATGATCAC TACAGTCATT 1020
GATGTGAGGA CGTCAGCAGC AGAGGGGCCT CCAGAGGACA TTTTCTTGCA CCCCAGGAGG 1080
CATTCCTGTC ATTTGTCCCC ACTGGGTCTG GGGCTGGGGC TTCTTTGTAC CTCTGAGGTA 1140
CAAAGTGGAA GCTCTGCCTG GCTGGCAAGA CCAGACCTGT TGTGGCGGCC AGGCTGTACC 1200
CACGCAGGGC CACTGCTCCT AGGGCACTGG GCTCCAGACA GAAAATGGGA AGGGACAGAT 1260
AAGCCTCTAT GAAAGGTGGC CAGGCACAGG AAAGAGGCCC TGCCCCCTTG AGAGGGAGGC 1320
CCTGCCCCCT TGAGAGGTTG GCCCCGCCTT GAGCATCCTT GTCAGGCAGA GATCTGGGCA 1380
GGACAGAAGA GAGGAGGTGC CTGGCTCAGT TTTGCTGCGA TCCCAATGGG TCACACGCCT 1440
TCTGGATCCC CCCAGAAGGT CTAGAATGGG GTCACCCCTC AAAACCTCCC TGGCTCACTC 1500
TTAGCTTGGA ACCATGAACG AGCTTGCTCC CACCCACATG GAAAGCAGCT GCCCTTCCCC 1560
TGGAGACATT TTCCACTTCT CTACCTCCAG ACCTCTGCTC ATGCTGTTTC CTCCACCTGG 1620
TAAACCTCAC TCTCTGCTGT GCTGTCAGAA AATGGCCAAC CTTTTGAGTC TCAGCTGAAA 1680
TGGCACTCCC TTTGCCCCAG CTTTAGTTTA ACAAGCATTT GTGCATGCTC TGGAGATGGG 1740
CTGTCCTGCC CTCATACACC CTGCTAGGGC CTAGCCAATG AGGGACAACC GGAAGTCTTA 1800
CCCTCCAGCC CCCACCCCGG AGACCACCTG TGTAGGACCC CCAGGGGTTG CCAGGATCCT 1860
CCCCACAAAC GGCAAAGCAC TCTCTATTTG GGGGAACAGC CCTTCTCTGG AATTGGGAGT 1920
AACAAGAGGA AGGGAGGAAG GGCGTCTTGT GAGAGGGAGG GGCCAGGAGG CCTGAGGGAG 1980
CTCTGGCGTG TGTTCCAGAA ACCCTTTGGG ATCAGAGACA AGATCAAAGA GGCAGCCTTC 2040
ATGAGGCTGT CCAGGGCCCT GGACATGGAC CCAGGAAAAT TGGCTGGGTG ACCTCAAGCA 2100
AGTTACTTGC CCTTGCTGAG CCTCAACCTC CTCATTTGTG AAACAGGGCT AGTACCCCCA 2160
ACCTCTGAAT GAGACGGTGA ACAGCCTTTG TGCATGGGAG GGGCTTGAGT CTGGGTACTG 2220
AGGGGCGAGC TGGGGCCTGA GCGAATGCTG CAAGTCCCCC AGGGCTCCTT CTCTGATGCC 2280
GTGTCTCAGA GCCCCCTCCC CTTCCTGCCT GCCCAGGGTT TCCCTTGCTA GGAGCAGTTT 2340
TAAAACTCCC CAGTACCTGG GCTATGAGCC ACAGCTTCTT AAAGTTCCCC ATCTCCTGCA 2400
GCAGGCTTAG TTGGACTGAG CCAGAGCCCA TCATTCACTG TTTCTGGAGA TTATCACAGT 2460
TTGCAGAAAC AGCAGGGCAC CTAGCAGGAA TCTGGCACAG GCTCCTCGCT AGTTGGGACT 2520
GGAACTGGGC CAGGACAGCA CCTCGTGTCC TCTAAAAGGA TCCACAGGGC CTTCCCTCTC 2580
TCCTTTCCCC TCACTCAGGC ACACTGGGGT TCCAGAGTTC TAGGGCCACA TCCCAGACAC 2640
AGGCACTGCA GTCTTGTCCC CACTGGGATA TGAGACACAG AAAGAACCCT GGGCTGGAGT 2700
CAGGGGAGGA TGGTCACTCC CCCTCTGTGG TTAAGGACAG AAACTCTGGA GCCAGACTGC 2760
TGGCGTTCAA ACCCTGGCTC TGTCATTTAC CAACTGTGAC CTTGAGTGAG TTACTTAACC 2820
TCTCTGTGCC TCTGTCTTCT CACCTGTAAA GTGGTGAATC ACAGTACCCG TCCCACCAAG 2880
TTGTTGGGAG GATGCAGTTA GTTACCCAGA AAGTGTTTGG AGTAGTGCCT GGTATGCAGT 2940
GAGCGCTGGC TTGGTTGGGT GAATGAATGG GTGCATGAAG GAATGAGTCA ATGCGTCGGA 3000
GCTCTGCTCT GTGGCACGAG GCCCTTCAGG ATCTGCCCGG ACATCAGCAC CTGCCATTGT 3060
CCCAAGCAGG TCATGATCAC ATCCTTCCCA CCAGCTTCCT TGGCTTGGCA TAACCTCACC 3120
ATTGCTGTTA GTCCCAAGAA CTCCTTCAAC ACATGCTTCA AATGCCACCT CCTCTCTGAA 3180
GCCTCTTCAA TCAGGACCCT CAGGGCTGTT AATGATAAAA ACCAAACCCA GCTGGATTTT 3240
CTTTTTTTTT CTTTCTTTTT TTTTTTTTTT TTGAGACGTT TTGAGACGGA GTCTCGCTCT 3300
GTCGCCCAGG CTAGAGTGTA GTGGCGCGAT CTCGGCTCAC TGCAAGCTCC GCCTCCCGGG 3360
TTCACGCCAT TCTCCTGCCT CAGCCTCCCG AGTAGGTGGG ACTACAGGCG CCCGCCACCA 3420
CACCCGGCTA TTTCTTGTAT TTTTAGTAGA GACGGGGTTT CACCGTGTTA GCCAGGATGG 3480
TCTCGATCTC CTGACCTCGT GTCGTGATCC ACCCGCCTCG GCCTCCCAAA GTGCTGGGAT 3540
TACAGGCGTG AGCCACTGTG CCAGGCCCCA GCTGGATTTT CTAACAAAAC AAACATCTTG 3600
GCTCACATTG CCTCAGAGGG AGGGAGGGAG GATCATCAGG CAGGAGACGA TCCAGGAGTT 3660
CAGATGCTGC TGCTAGATTT CTCTCCCCTG CCTCATCTTC CATGCCTCAT CTTCCCCTTG 3720
TGTGTTACCT TCACTCTCAT CTCTGAGATT AGACATCCTT CACACCCAGA GAATTCGGCC 3780
AGGCTTACCT TGTGGTAGCT GAGAGCCCTA GAGAAAAAAA ACCTTCTCTC TCCCTGGGCT 3840
GAATTAGAAA GTCCCAGGGA AGAACTCTGA TTGGCCAGGC CTGTTTCCTG TGCCCTCCCC 3900
TGTGACTTAG TAGAGGTGGG GCCTGATGCT GTGATTGACA GCCTGGTTAA TCGGCTAAAC 3960
TCAGTAGGCG TGTCCCATGC ACCACAAGGA ATTGGGGAGG AACAATTCCC AAAGGAAGGA 4020
GGTTGCTGTT AGCAGAAGAA AGGCAAAACA ACCTGTGTCC ACATCATCCC TCCTGCCACC 4080
TCTGGCCCTG TGCTTTCACT GCACTCTGCA CACACCCCCA GCAGACCCCA CCCGAGCTTC 4140
CAGGGATGAT TTGGGTACTT GGGTATGGGT GACTGTCCCT GCCACTGGAC GATGAAGTCT 4200
TAAAGGGCCA AGACTCTGGT CACCTTGGCT CTCCCAGCCC TCTGCTCTGT CCCTGATCAT 4260
AAACTACTTT TGACGAACGA AGAAAACGAA GGATCAAGGA ATAGAAGGGG TTGTGTAAGG 4320
GGCCAACCAG GATGAAAATC TTCATCTAGG CTCTTCCAAC CCTACCCTGC AGCCTCCTCC 4380
CTCAACCCAC AATCAGCAAC 4400