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

TagContent
EnhancerAtlas ID
HS182-14171 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr20:56055530-56058200 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs61458527chr2056057093hg19
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFAT5MA0606.1chr20:56057866-56057876ATTTTCCATT+6.02
NFATC1MA0624.1chr20:56057866-56057876ATTTTCCATT+6.02
NFATC3MA0625.1chr20:56057866-56057876ATTTTCCATT+6.02
POU2F2MA0507.1chr20:56056774-56056787ATTATTTGCATAT+6.14
ZNF263MA0528.1chr20:56056083-56056104GGGGGAGGAAGGGGCTGTGGA+6.21
ZNF263MA0528.1chr20:56057164-56057185AGGGGAGGAGAGGGGGAGGAG+6.38
ZNF263MA0528.1chr20:56057159-56057180GGAGAAGGGGAGGAGAGGGGG+6.62
ZNF263MA0528.1chr20:56057156-56057177GAAGGAGAAGGGGAGGAGAGG+6.76
ZNF263MA0528.1chr20:56057175-56057196GGGGGAGGAGAGGGGGAGGAG+7.2
ZNF263MA0528.1chr20:56057186-56057207GGGGGAGGAGAGGGGGAGGAG+7.2
ZNF263MA0528.1chr20:56057197-56057218GGGGGAGGAGAGGGGGAGGAG+7.2
ZNF263MA0528.1chr20:56057208-56057229GGGGGAGGAGAGGGGGAGGAG+7.2
ZNF263MA0528.1chr20:56057219-56057240GGGGGAGGAGAGGGGGAGGAG+7.2
ZNF263MA0528.1chr20:56057167-56057188GGAGGAGAGGGGGAGGAGAGG+7
ZNF263MA0528.1chr20:56057178-56057199GGAGGAGAGGGGGAGGAGAGG+7
ZNF263MA0528.1chr20:56057189-56057210GGAGGAGAGGGGGAGGAGAGG+7
ZNF263MA0528.1chr20:56057200-56057221GGAGGAGAGGGGGAGGAGAGG+7
ZNF263MA0528.1chr20:56057211-56057232GGAGGAGAGGGGGAGGAGAGG+7
ZNF263MA0528.1chr20:56057222-56057243GGAGGAGAGGGGGAGGAGAGG+7
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_43635chr20:56046678-56058511MM1S
SE_54280chr20:56056009-56056835Spleen
SE_54280chr20:56057141-56058269Spleen
SE_54690chr20:56055043-56057186Stomach_Smooth_Muscle
SE_58384chr20:55990107-56074254Ly1
SE_59384chr20:56044028-56070796Ly3
SE_59605chr20:56000010-56074239Ly4
SE_67245chr20:56046678-56058511MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr205605596456056165
Number: 3             
IDChromosomeStartEnd
GH20I057480chr205605535856057418
GH20I057483chr205605768156057830
GH20I057482chr205605796156058949
Enhancer Sequence
CCCTGGGTGT AGGACCTCAG GTGAAGGGTT ACTCAATTTG GGGCAGCTTC CCTAAGCCAT 60
GATTGTGCCG CACGCATGGC TGGCAGCATG GATGTCAGTG TGGGGAGGCC CAGGCCCTTG 120
GAGGAGGCTG AGGCAGCCTT GTCTGGGACC CCAGGTACGC CTCCAGCCAT CTTCCCCACA 180
GCCCCTTCTC TGAGCGCGCA GCCATCACCC CAGACCCGGG CTGATATTTT TAGCACACAG 240
GCACCCTGCA CGGCCCTGTA CACTCTGACC AAATTTAGAA ATCTCAAGAG ATCTTTGCTT 300
TTCTACGCCT TCAGAAGGAG CAATGAATGA AAAGGCTCCC AGCCTCCGGT TTAGTGAGAG 360
CAAACCCTCC TGTTTGCAGG GCTCTCTCTG GTAGGGAACC CCAAGCTTTA CTGTGCAGTG 420
AAAAAAAGCC AGGTGCAGAA TCCTGTGTGT GTTTTGGGTC TACGGTAGCA AATGCAAAGC 480
AACCCCTGCA CCGTGCACGT GTGTCTGAGT CAGCACAGCC AGCAGCGGGG CGTGGAAGGA 540
GCCCCCCGCA AGTGGGGGAG GAAGGGGCTG TGGAGGTGAT TACCTCACTC TCATGCAGGG 600
CTGAATATTA CTGTTTCCCC TGTTAAACAA GGGTGTATTA CTTCCGAAAT CTGACAACCC 660
CAAGCACCAA AAGGTTTAAA AATATCTCGA GATTGTAAAG CCTCCGACAG AATGCTGAAA 720
CAGGATTGCA CAGTTGACCA GGAGCTTCTG AGGTTGTGGC GGACCCTCCA TGTTTCTGAC 780
TGCCGGACAG TCACAGCCCC CTCTTCCCTA ATGCCACCAG ATGTTCCCTG GGACACCTGC 840
CCCCAGCTCT AGTCCACATA ATGCTGCCCT CCACCTCCAG ACCCAGGGGA GGGGAGTGGT 900
CAGGGCCGGC CAAGCCAAGC ACCGTATGGC CCCTGGTTCA GGACATCGCT GGGACCCAGA 960
GGCCAGAGAC CTTCAGCTGG GATCCCCAAG GATCCCTTGG GACCCCTGGG ACTGTTGTCC 1020
ACCTCTGTGC CACCAGGAGA GGAGAGCCCC ACTAAGACTG GAGTGACACC GGAAGGTGCA 1080
ACCAAGAGCA GGCAGGGAGA ACACGGAGTG CAGGCGCTGC CTGAGCCCCT GCCCTGGGCT 1140
GTGTCGGGGG AGCTACTGTG GAACTTTCTG TCTATGCAGG CTCAGCAGGC CACAGTGTGC 1200
ACCACCCGGC TCCTGCCAGT GAACCTACAA ACGCTGATGG CTAGATTATT TGCATATGTG 1260
TTGTTAAATA TGGCCAATAT TAAAATTAAA TGATACAAAC ATGTAATTAA AGGAATTACA 1320
TTAAAAACAG AGATAATAGC TCCTCAGGAC ACCTCACTCC CTAATTAGCA TACTGCACTT 1380
CACCATTCCC CAGGCTCTTG GGGTGCCACC TCGGCTGCAT TTGGGGGAAG GAAATGCTTT 1440
AGGTCTGGAC GTGCATTCCT GTGCGTCCTC TGGATAGCAG GAAATCTGCC AGCATGGAAA 1500
TGGCAAATGC TACAAACAGG GGTCCCCCCA AAGCCATTGC TTCCCAGCAT GCCTCTGAGA 1560
GAAGCCCTGT AACACAGGCC AGGGGGCACC TGCTCTGCAG GACCCCAAGC AACAGGAAGG 1620
AAACAGGAAG GAGAAGGGGA GGAGAGGGGG AGGAGAGGGG GAGGAGAGGG GGAGGAGAGG 1680
GGGAGGAGAG GGGGAGGAGA GGGGGAGGAG AGGGCAAGGA GAGGTCTTCG GCATCCTTAT 1740
GGTGAAAACC ACATTTTCTC CTCCCCATTT CCCTGGTAGC TGGGAAGCGC ATTCAATTAA 1800
CGTGTATTGA TTGGCTTGAG GAAATCGGGC TCCCAGAAGT CTAGGGCCTT GCTTAAGGTC 1860
ACCTAGCGGT GGGGCAGGAA CTGGGACACA GTTTTAATTT GACTCCGGAG CCCTGGACTG 1920
GCCTTGTAAT TGGTACTTCT TGTGCAGTGC TCACGGACAC CTCAGCTGAA TGAAGGCCGT 1980
GCAGGTGGCT GGACAGAAAC GCCCTGTAGC CCGCATCCCT CACGTTCAAG GCTTCTGTTT 2040
TTTCAGCACT CATTTCTAAG TGGCTTGCAG CCTTGCAAGA TGAATTGTGG AAGTGCATGG 2100
GCACAGTACT TAAAAACATA GAGTCCCGAG CTGAGGCAGG TCTGCCCTTT CCAGTTATTT 2160
TCCAATCCTT GTGATTACAA AGAGGTTTCT TATTTAGGGG TGAGCCTGAC TTTCACACTC 2220
GGGCAGGCTC CACTGGCAGC CAGCCTCCTG TGTCCCAGCC TCCAACAGAA GTTAAAGACA 2280
CGAGGAGGGT TCAATGCATT CACTTTGGGG GATCCCTCCT GCTTATTAAG AAAATGATTT 2340
TCCATTTTTG GTAACAGTAG AGTTTTCTTT TAAAATTATT TAAGTAAATT TGGGGAGCAA 2400
ATGCTACAGA TAGTTATGGA AGGCATCCTG AGCTGATGGG CAGTTGCTGG ATTTGATGGG 2460
AAACCAGGAT CCAATTCAAT TTCCCAGAGA ACCCGAGGCC TGGCGCGGGC AGGGAGGGTC 2520
AAGGAAGGGA GGAGCCCAGG GTCCGGCCCT CGGCCCCAAT CAGGGAATGC AGCTGCCTCA 2580
GAAAATGCTG GCTTTCATAT GTCAGGGACA AAAGGGACCC TTTTTTCTCC CCTTTTTTTA 2640
GTTAGAAGGA AACCTTTGAG CCATTTATAA 2670