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

TagContent
EnhancerAtlas ID
HS091-11355 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr12:133045780-133049500 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs142425959chr12133047545hg19
rs75588192chr12133048600hg19
TF binding sites/motifs
Number: 52             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr12:133047286-133047304GGAGGGGAGGGAGGAGGG+6.27
EWSR1-FLI1MA0149.1chr12:133047170-133047188GGAAGGGAGGAGGGGAGG+6.66
EWSR1-FLI1MA0149.1chr12:133047166-133047184GGAGGGAAGGGAGGAGGG+7.28
EWSR1-FLI1MA0149.1chr12:133047149-133047167GGAAGGGAGGGAGGAGGG+7.46
MEOX1MA0661.1chr12:133048257-133048267GTTAATTAGC-6.02
POU2F2MA0507.1chr12:133048954-133048967AAATGCAAATTAA-6.25
SP2MA0516.2chr12:133045836-133045853GAGGGGGTGGGACATAT-6.24
SPI1MA0080.4chr12:133047843-133047857AAAAAGCGGAACTC+6.25
Stat4MA0518.1chr12:133049395-133049409TCCCTTCCTGGAAA-6.2
ZNF263MA0528.1chr12:133047147-133047168GGGGAAGGGAGGGAGGAGGGG+6.15
ZNF263MA0528.1chr12:133047168-133047189AGGGAAGGGAGGAGGGGAGGG+6.22
ZNF263MA0528.1chr12:133047414-133047435GGGGAAAGAAGGGGAGGGGAG+6.22
ZNF263MA0528.1chr12:133047264-133047285GGAAAAGGAAGGGGAGGGGAA+6.28
ZNF263MA0528.1chr12:133047053-133047074GGGGGAGGGGAGGGAAGAAAT+6.36
ZNF263MA0528.1chr12:133047141-133047162AGGGGAGGGGAAGGGAGGGAG+6.36
ZNF263MA0528.1chr12:133047180-133047201AGGGGAGGGAAAGGAAGGGAA+6.54
ZNF263MA0528.1chr12:133047300-133047321AGGGGAGGGAAAGGAAGGGAA+6.54
ZNF263MA0528.1chr12:133047267-133047288AAAGGAAGGGGAGGGGAAGGG+6.63
ZNF263MA0528.1chr12:133047432-133047453GAGGGAAGGGGAGGGGAGGGA+6.63
ZNF263MA0528.1chr12:133047447-133047468GAGGGAAGGGGAGGGGAGGGA+6.63
ZNF263MA0528.1chr12:133047462-133047483GAGGGAAGGGGAGGGGAGGGA+6.63
ZNF263MA0528.1chr12:133047477-133047498GAGGGAAGGGGAGGGGAGGGA+6.63
ZNF263MA0528.1chr12:133047172-133047193AAGGGAGGAGGGGAGGGAAAG+6.67
ZNF263MA0528.1chr12:133047483-133047504AGGGGAGGGGAGGGAAGGGAA+6.71
ZNF263MA0528.1chr12:133047146-133047167AGGGGAAGGGAGGGAGGAGGG+6.72
ZNF263MA0528.1chr12:133047634-133047655GGAGGAAAAGGGAAGGGGGGG+6.73
ZNF263MA0528.1chr12:133047428-133047449AGGGGAGGGAAGGGGAGGGGA+6.74
ZNF263MA0528.1chr12:133047443-133047464AGGGGAGGGAAGGGGAGGGGA+6.74
ZNF263MA0528.1chr12:133047458-133047479AGGGGAGGGAAGGGGAGGGGA+6.74
ZNF263MA0528.1chr12:133047473-133047494AGGGGAGGGAAGGGGAGGGGA+6.74
ZNF263MA0528.1chr12:133047408-133047429AGGGGAGGGGAAAGAAGGGGA+6.77
ZNF263MA0528.1chr12:133047273-133047294AGGGGAGGGGAAGGGAGGGGA+6.9
ZNF263MA0528.1chr12:133047036-133047057AAGGGAGGGGAGGAGAGGGGG+6
ZNF263MA0528.1chr12:133047129-133047150GAGGGAAAGGGAAGGGGAGGG+6
ZNF263MA0528.1chr12:133047396-133047417GAGGGAAAGGGAAGGGGAGGG+6
ZNF263MA0528.1chr12:133047151-133047172AAGGGAGGGAGGAGGGGAGGG+7.07
ZNF263MA0528.1chr12:133047423-133047444AGGGGAGGGGAGGGAAGGGGA+7.19
ZNF263MA0528.1chr12:133047438-133047459AGGGGAGGGGAGGGAAGGGGA+7.19
ZNF263MA0528.1chr12:133047453-133047474AGGGGAGGGGAGGGAAGGGGA+7.19
ZNF263MA0528.1chr12:133047468-133047489AGGGGAGGGGAGGGAAGGGGA+7.19
ZNF263MA0528.1chr12:133047032-133047053GGGGAAGGGAGGGGAGGAGAG+7.23
ZNF263MA0528.1chr12:133047279-133047300GGGGAAGGGAGGGGAGGGAGG+7.23
ZNF263MA0528.1chr12:133047283-133047304AAGGGAGGGGAGGGAGGAGGG+7.34
ZNF263MA0528.1chr12:133047292-133047313GAGGGAGGAGGGGAGGGAAAG+7.53
ZNF263MA0528.1chr12:133047288-133047309AGGGGAGGGAGGAGGGGAGGG+7.56
ZNF263MA0528.1chr12:133047175-133047196GGAGGAGGGGAGGGAAAGGAA+7.63
ZNF263MA0528.1chr12:133047295-133047316GGAGGAGGGGAGGGAAAGGAA+7.63
ZNF263MA0528.1chr12:133047163-133047184AGGGGAGGGAAGGGAGGAGGG+7.66
ZNF263MA0528.1chr12:133047041-133047062AGGGGAGGAGAGGGGGGAGGG+7.79
ZNF263MA0528.1chr12:133047155-133047176GAGGGAGGAGGGGAGGGAAGG+8.09
ZNF263MA0528.1chr12:133047158-133047179GGAGGAGGGGAGGGAAGGGAG+8.36
ZNF263MA0528.1chr12:133047044-133047065GGAGGAGAGGGGGGAGGGGAG+8.4
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_10775chr12:133042196-133047061CD19_Primary
SE_10775chr12:133047106-133048987CD19_Primary
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr12133046200133047046
chr12133047564133048151
chr12133047496133048192
Number: 2             
IDChromosomeStartEnd
GH12I132467chr12133043681133046986
GH12I132470chr12133047235133049786
Enhancer Sequence
AGATAAAATA TGTATAGTAG GTCTGGGGTG ATTCATGCCA TGGAGAAAAA GTAAGGGAGG 60
GGGTGGGACA TATGGGGCAC AGGGCACCAG GGGGGCCAGG AAGGGTCCCC ATGCACAGTT 120
ACGGCCAACT GACCTTCAGC AAAGGCGCCA AGGACACACG ACGGGGAAAG GGGCATCCTC 180
AATAGGTGGT GCTGGGAAAA GTGGAGGAGG ATGAAAGGGC CTCATCCGAC ACCACCTACG 240
AAAATCAACT CAACACGGAT TAAAGATTCA AACCTAAGAC CCGACACCAT AAAACTCTTA 300
GAAGAAAACG TAGGAGGAAA ACTTCTTGAG GCTGGTCCGG GCAATGATTT TTTTAAAATA 360
TGGCCCCACA AGCACAGGCA ACAGAAGCAA AAATAGACAG TGAGAGTGCA ACAAACCAGA 420
AAGCTTCCGC AAAGGAAACC AACAGAGTGA AAAGGCAACC CCCAGGGGGA GGCGGGGGTA 480
TTGGCAGGGA AAAGGCAGAA CCCACGGGGA GGTGGGGGTA TTTGCAGGGA AAAGGCAACC 540
CCCATGGGGA GGTGGGGGTA TTGGCAGGGA AAAGGCAACC CCCATGGGGA GGCGGGAGTA 600
TTTGCAGTGA AAAGGCAAAA CCCCAGGGGG AGGCGGGGGT ATTTGCAATC CATGTATATG 660
ATGAGGAGTT AATTTGCAAA TTGTAGAAGG AATTCAACTC AATAACAAAA ACAAACAAAA 720
AAAATTTTAA AACGTGCAAA GGACCTGAAT CTGCGTGTCT CGAAGGAAAA CATGTAAGTG 780
GCCGAAGTGT AGACGAAATA ACGTCCAGCA TCACTAATCA TCAGGAAAAT CAAATAAAAA 840
CCACAGGAGG TACCAACTGG CACCTATTGG GATGACTGTC ATCAAAACGC AAAAGATAGC 900
GAGTGTTGGC GAGGACATGG AGGAAAGGGG CCCGTTGCAC TCTGTCCCTG GGAACGTCGT 960
TGGCACAGCC ACCATGGGAG ACGGCAGGGA GGTTCCTCAA AAATGTGGAA ATAGAGCTCC 1020
CACCTGATCC AGCAATCCCA CTGCTGGGTG TATATCCAAA GAGTTGAAAT TAGCGTGTAG 1080
GAGAGGCGTC TGTACCCTCG TGTTCATCGC AGCACTGTCC CAGCAGCCAG GACACGGAAT 1140
CAACCCAAGT GTCCATCAAC GGATGCATGA ATGAAAATAT GTGAGAAATA TACACACACA 1200
TGCATGCACA CACACACAGG AGTGTTATTC CACAGGAGGG AAAGGGAAGG GTGGGGAAGG 1260
GAGGGGAGGA GAGGGGGGAG GGGAGGGAAG AAATACACAC ACATGCATAC ACACACACAC 1320
ACACACACAC ACGAGTGTTA TCCCACAGGG AGGGAAAGGG AAGGGGAGGG GAAGGGAGGG 1380
AGGAGGGGAG GGAAGGGAGG AGGGGAGGGA AAGGAAGGGA AAGGGAGAAA TATACACACA 1440
TGCATATATA CACACACACA CACACAAGCG TTATTCCACA GAAGGGAAAA GGAAGGGGAG 1500
GGGAAGGGAG GGGAGGGAGG AGGGGAGGGA AAGGAAGGGA AGGGGAGAAA TACACACACA 1560
TGCATACACA CACACACACA CACACACACA CACACACACG AGTGTTATTC CACAGGGAGG 1620
GAAAGGGAAG GGGAGGGGAA AGAAGGGGAG GGGAGGGAAG GGGAGGGGAG GGAAGGGGAG 1680
GGGAGGGAAG GGGAGGGGAG GGAAGGGGAG GGGAGGGAAG GGAAGAAATA CACACACATG 1740
CGTACACACA CACGTATACA CACACATGCG TACACACACG TATACACACA CATGCGTACA 1800
CACACGCGTA TACACACACA TGCGTACACA CACATACAGG AGTGTTATTC CACAGGAGGA 1860
AAAGGGAAGG GGGGGAGAGA GAGAGAGACA GAGAGAGAGA AAGGAGAGAG AGAGAAGGGA 1920
AGGGAAGGGA GGGCAGGGCA GGGCAGGGCA GGGCAAGCCC GCCATTTGTG AGGACACGAT 1980
GAACCTGAAG GGCATTTGTG GTAAGTGAGA TAAGCCAGGC ACAGAAAGAC AAACAGCACA 2040
TGGCCTCACT CGAGTGACGT GTGAAAAAGC GGAACTCACA GAAGCAGAGT GAACAGTGGC 2100
TGTCAGGGCT GGAGGGGACC GGGAGTTGAG GGTCACAGGG AACAAAGGTG CAGTTATGAG 2160
ATTAGCGGGT TCTAAGATGT AATGAACGTG GTGACTACAG CTGATAAGAA TGTGTCCTTT 2220
ATTTATTTAT TTTGAGATAG GGCCTCCCTC TGTCGCCCAG GCTGGAGTGC ACCGCAACCT 2280
CCGCCTCCCA GGCTCAAGTG ATTCTCCAGC CTCAGCTTCC CAAGTAGCTG GGACCACAGG 2340
TGTGCACCAC CACGTCCAGA TAATTTTTTT ATATTTGTAG AGACAGGGTC TCACTATGTT 2400
GCCCAGGCTG TGTGTCCTCT ATTTAAAATT TAGTGTTCTC ACCACAGAAA GAAGTAACCA 2460
TGTAAGGTGA TGGGTGTGTT AATTAGCCCA ATTGTGGGAC TCATTTCACA ATGCCTACGT 2520
GTGTCAGGTT GTGATGCTGC ATACCTTGAG TGCACACCGT CCTGAATTGT CAACTATACC 2580
TCAATAAAGC TGGAGAGAGA GAAAGAAAAG AAAAGGTATC CTGGGACGGT GACGTGGGTA 2640
ACGGGCCCCA GGACACTCAC AGAGAGAGGG AATGCAGGTG CAAAGGCCCC GGGGCAGTGA 2700
CAAACAGGAA GCAGGAAGAA GGGCCAGGGT ACGGGGATGG GGCCTGGCCG ACCTCCATGC 2760
CCAGAGCCTT CCTTTCCCGA GTGGGAAGAG CCGGGAGGTT CCTGCGGAAC AAACGCCTGG 2820
GTTGAGGTGG CGCAGAGCCC TGAGGGGGCT CAGGCGAGGG TCCAGGCCAG GTGGGCAGGC 2880
GGGGGCAGCA CTCTGCAAGG GCAGGAGCCA TCAGGAGAGC ATCGGCTGTC CCTGGGGAAG 2940
GCCCCTCATG GAAGGAGTGA GCCGGTAACA GGGAGTTGGG GGGCGGATTT GGGGGTCAAG 3000
CACAGGCTCC TGAGCGGCCA GGCGGTGAGC GTCTGCACTG CCCTGCAGAC CTCAGGCATC 3060
ACTGGCATCT TGAAGCAGAA ATGACATAAT CAAGTTTTGC TTTAGGAAGA AATATCTCTA 3120
TCCCCAAAGC CAGCAAACAT ATGAAGAGAT GCTCGAAATC ATCAGTCATC AGAGAAATGC 3180
AAATTAAAGC CACCACGATG ATCCCGTCCC ACCATCTAGC TGCCAAGATG AGAGGCCGGA 3240
TCTGCCAAGT CCTGGCAGGG GTTTGGGAGC ATCCCCTGGA GGGACGGAAC CCTCGTCCAC 3300
TGCCCCCTGC CCGAGGAAGG GGTGAGGCGG CCCTTAGGGA GAGCAGCTGG AGCCGGGGAA 3360
GGGCTGGGAA GTCCTCACCC AGGTCCATGG GGGCAGGTCC AAGGCTGCGC ACCGAGGCGC 3420
CATCATGGAC CCCTTCTCTG CCGGCCGCCT GCAGTTCTGG GGCTCAAGCA CAGGGTGCCC 3480
TGCCAGGGAA GGTGCGGCAG GAGATCCAGC CCCTCCACCA AAGCCTGCCT GGAGAGAGAG 3540
GAGGGCCTGT TCCTCATCTT TCTTCTGATT TACACAAAGG CACGATGTGG GCCGGCAGGA 3600
GACCTGAACC CGGGGTCCCT TCCTGGAAAG TGCGTGGGCA GCTCGTGAAC CCGGTGTCCC 3660
CTCCTGGAGA GGACGTGGGC AGCTCGTGGA CCCGGGTCCC TTCCTGGAGA GGACGTGGGC 3720