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

TagContent
EnhancerAtlas ID
HS093-20154 
Organism
Homo sapiens 
Tissue/cell
HL-60 
Coordinate
chr21:36397560-36400150 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56117721chr2136398586hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFAT5MA0606.1chr21:36399848-36399858AATGGAAAAT-6.02
NFAT5MA0606.1chr21:36399855-36399865AATGGAAAAT-6.02
NFATC1MA0624.1chr21:36399848-36399858AATGGAAAAT-6.02
NFATC1MA0624.1chr21:36399855-36399865AATGGAAAAT-6.02
NFATC3MA0625.1chr21:36399848-36399858AATGGAAAAT-6.02
NFATC3MA0625.1chr21:36399855-36399865AATGGAAAAT-6.02
RORA(var.2)MA0072.1chr21:36397938-36397952TATATTTAGGTCAA+6.61
ZNF263MA0528.1chr21:36399432-36399453GGGGCAGGGGGCGAAGGGAGG+6.02
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_12094chr21:36397718-36402514CD3
SE_12952chr21:36397410-36401163CD34_Primary_RO01480
SE_13349chr21:36396290-36403486CD34_Primary_RO01536
SE_14088chr21:36397200-36403592CD34_Primary_RO01549
SE_14594chr21:36396664-36402689CD4_Memory_Primary_7pool
SE_15489chr21:36397436-36401545CD4_Memory_Primary_8pool
SE_16161chr21:36397923-36401779CD4_Naive_Primary_7pool
SE_16407chr21:36397625-36401471CD4_Naive_Primary_8pool
SE_17113chr21:36397447-36401365CD4p_CD225int_CD127p_Tmem
SE_17718chr21:36396331-36403673CD4p_CD25-_CD45RAp_Naive
SE_18060chr21:36395220-36403718CD4p_CD25-_CD45ROp_Memory
SE_18260chr21:36396030-36403534CD4p_CD25-_Il17-_PMAstim_Th
SE_19195chr21:36396261-36402495CD4p_CD25-_Il17p_PMAstim_Th17
SE_20417chr21:36397066-36402490CD56
SE_20980chr21:36397481-36402434CD8_Memory_7pool
SE_22199chr21:36397604-36401949CD8_Naive_8pool
SE_22731chr21:36396743-36402539CD8_primiary
SE_25349chr21:36395206-36403524DND41
SE_31093chr21:36397076-36402460Fetal_Thymus
SE_39356chr21:36396262-36402464Jurkat
SE_49891chr21:36395463-36399170RPMI-8402
SE_49891chr21:36399276-36402442RPMI-8402
SE_54173chr21:36397498-36401669Spleen
SE_62936chr21:36397339-36424568Tonsil
SE_66240chr21:36396262-36402464Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr213639770836397817
chr213639796036398200
Number: 1             
IDChromosomeStartEnd
GH21I035024chr213639662836403251
Enhancer Sequence
TCTCCATGAG GACCTCAAGG TAAATAATAG GAATCGATCA TTCATCAATC TGGCCTGGCC 60
CCGGCCCACT GAAGAAAGTT CCTTCTTGAG TGCATTCAAA GCTCTCATGG TCCAGCCCTG 120
TTCAACCTGA GCAGCATCCT ATCTGCTCCT CCCCCAGACG TTCCGATGCC CTGCACCAGA 180
TTCAAGAGAG AGCCAAGTTC CCCAACAGGC TATGCACGTG GCTATTAACA CCCAGCACAC 240
GCTATCCCTG GCCAGCTCTC TCCTTCTTCC CTAAGAATTA AACATTCTTT GGCCTGAGTT 300
TTCCTCCTTT ATGTCACCAT AAAGTTGAGT TATTCATTAT TAGGGTCTAT ACATGAGTAG 360
CCAAAATATA CGGGTCTCTA TATTTAGGTC AAGGGGCCTT CAGCAGGAGA ACATGAATAA 420
TTAGGAGTGA GGCCATGAGA CAGAGGAAGA AAAGCTCATA GGAATGGGAA GACAGCCTCT 480
CAGATGAGAG GTGTGCGGAG TGATTGCTGT GAGGAATTGC TCAATAGGAA AGTTAGCCAA 540
CCTGAGGACG TTTCTAGGGG AGGAAAAGGG AAACTCATAT GGTTCTCTGC TAATTCTTAA 600
AAATAAGGTA GATTCTTACT CATCTAGGGT GCTTGCTCGT TATGAACACA GGAAGATTAA 660
GGAATGAGTA TGGACTGTTT CTACTCTATG TTTTCGGACA AGAAGAATAA TAAAAAAGCA 720
CTGGGTAGCT GGAACAACTG CAGAGGCCCC AACAATGATG GAGACTTTCT GGTGCACCGT 780
GGCACAGGGG TCTCTTCCAA AGGGACTCAA TCAACCCCAA CAGGCATCAT CTTCTGTGAC 840
TCAAGATGTC CTTTTTAGGA GTGCTTGTAC TTTTTAATGC TCAGAGAAGT TCGTATTACT 900
GATTCGGGAA CACTGAGTTT TTCAGCTCCT GTAAAACTAT TTTCAGGTTT ATTTTCAAGT 960
ACATTCTTTA CCTCGGGGGG TCAAATCTTT TGGTTTCCAG TGAATATCGT GGTTATACCT 1020
GTGGTTACCC ACTGACTTCT CATCTGCCTA GCTTATCTGA TAACAGGCAA ATGGGGAAAG 1080
AGGCTTTAAT ACCCCTCAAA AGGGGAAGAT TGATAATTAG TTATTCACCG CATAGAATCA 1140
GGCCAGGTCA ACTCTCTCCA AGAAGAAAAG CAATCTGGAT ATTGCACTTT GGGGTCCCTT 1200
TTCATTTTGG CATTACAGGC CTCATGAGGA TGTAGTCTTT CTGTATTTCT TTCTTTCTTT 1260
TTAAATTGTT ATTTATTTAT TTATTTTAAC CAGGTCAAAG CATTACATAC TGCAGAAGAG 1320
AAAGCAACTT CAGCTTCTCT TAAACGGTGT CATTTTCATG ACAGCTCGTA AATTTTGGCC 1380
TCCTATGGGT CCAGGATCTG CGCGCATCCG CCCGGGGACT TGTTGGTGGA TCCATCCCTC 1440
ATGGCGGAGC AGCAAGGGGA TCCTTTAGAA AAAGCAATGG GCGAAGTAAC TGAAAGAGCG 1500
ACGCAGAAAG CAACAGCCAG AAACGGCGGG GACGCGAGCG GCCCAGACAG GAAGGGAGGC 1560
GGTGGCGCAG CTCTGGTGCG CAGCGCGCCG CAGCGACGGA ACTTCTGCAA AAGCTGCCTG 1620
CCCGCGCGTT ATCAGCGGCG CGCAGGCCTG TGGTTTTCTC GCTCTCGCAA CCCTGCTTTA 1680
ACTGCCGGTT TATTTTTCGA CAAACAGGAT GCCTCCATCT GAGGCTGTCA GCATCCCAGG 1740
CTCTTTGAAA GAAAAGAAGT AGAGCGGCCC CACCCTAGAG GCAAGGACGG GGTCTGTGTC 1800
AAGAGGCTTC CCAGAGAAGT GAAAACTCTG CAGGTGCAGC CGCTGGGAGA GCATCAAGAA 1860
GGGCAGGGTG GAGGGGCAGG GGGCGAAGGG AGGGGGTGAA GCCCGCACCC TACCCCCACA 1920
TGAAACTGAT TCCACTACCC CATCTCTGCA AGCGTCCAGA GGCAGAGAGG CCAACATTTC 1980
GGGGACAGCT TGGAGGCGGG AGATTTAGGC AGGGCTCCTT AAACTTTTAT GTGCATGAAA 2040
ATCAGGCCAA TCACGGGGCT CTTGAGCAAA TGGGGACGAT GATTCAGCAG GTCTGGGCTG 2100
AGGCCTCAGA TTCTGCACTT CTAACAAGTT CCCAGGTGGT AGTGATGCTG CCAGTCCAAA 2160
GACCACACTG TGAATAGCAA GGCGTCGTCG GGACAGTCTG CTTTAGAGTA AAACCTAATA 2220
GATGTGCAAA TATTTAAACC AAGCTGTATT TATTCCTGAG GCCCTGGTTT AACTGGAGCC 2280
ACCTTGCTAA TGGAAAATGG AAAATGAAAT TCCTTTAGGT TCCAAAGGGA AGGAAAGTTT 2340
GAAATGGTTA AGGTATTTAA AAAATCCTAG TTGGGAGTGG CCTTGGGGAT TCGGGAGAGT 2400
TGAAGTTAGG TTCTGAGCCA AGAGATGGGG GAGGAAGGGT GGGATGTGGC AAATAAATAT 2460
AAACACACAC ACACAAACCC CAGCCCAACC ACAGGTTCTT TCCTATCAAT GAAACATTTG 2520
CATCTTGCAG GTAGAACTCA CACGTGTCCA CATTTTTCAG AAGTTGAATG GTTTTGTGTA 2580
ATGGTACAGA 2590