EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS187-15929 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr21:45626260-45629080 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs55708341chr2145627581hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr21:45627639-45627650GGATGACTCAG+6.32
JUNBMA0490.1chr21:45627639-45627650GGATGACTCAG+6.14
Myod1MA0499.1chr21:45627865-45627878GGGGGCAGCTGCT-6.03
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00694chr21:45627172-45628515Adipose_Nuclei
SE_03880chr21:45627327-45628971Brain_Anterior_Caudate
SE_04775chr21:45626030-45629668Brain_Cingulate_Gyrus
SE_05779chr21:45625585-45629669Brain_Hippocampus_Middle
SE_06690chr21:45625851-45629031Brain_Hippocampus_Middle_150
SE_07737chr21:45627279-45628360Brain_Inferior_Temporal_Lobe
SE_10305chr21:45623380-45628791CD19_Primary
SE_11616chr21:45622912-45630050CD20
SE_24239chr21:45625900-45626559Colon_Crypt_2
SE_24239chr21:45626613-45628029Colon_Crypt_2
SE_24239chr21:45628152-45628712Colon_Crypt_2
SE_30176chr21:45627362-45628673Fetal_Muscle
SE_31647chr21:45625794-45628702Gastric
SE_33667chr21:45621645-45627097H2171
SE_40890chr21:45625813-45629023Left_Ventricle
SE_42286chr21:45625817-45628837Lung
SE_48538chr21:45625974-45628773Psoas_Muscle
SE_50113chr21:45625833-45628971Sigmoid_Colon
SE_51445chr21:45624818-45629069Skeletal_Muscle
SE_52463chr21:45625843-45628782Small_Intestine
SE_56643chr21:45626252-45630945u87
SE_59125chr21:45557380-45640832Ly3
SE_61237chr21:45557180-45641526HBL1
SE_61527chr21:45545883-45641600Toledo
SE_62281chr21:45556124-45641130Tonsil
SE_65639chr21:45625460-45628847Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr214562660045628736
Number: 2             
IDChromosomeStartEnd
GH21I044205chr214562527245628706
GH21I005055chr214562595545628553
Enhancer Sequence
TTTCTAGGCC CCGCCTGTGG TCCTCTGTTG CAGCAGCCTG GACAGTCTGG ACTGCCTGGA 60
CAGCATGCAG ATGGGCTCTG CCCGCGGCTG CCCACGAGTT CCCACCGCCC GCCCGTCCGT 120
GGGAGAGCCA GTCCTCGTAT GTGAAGCGTA CCTGTATCCC TTTACTCCGC GTACACAGGT 180
GCCTTTGTCA CTTCTCCTTT GACCTGGCTG GCACATCTTA CCGGTTTCTG CGCTAACAAT 240
GAGTTGAAGG AAATCTTGAA CGCGCGTTCA TTTTATATCG GTATCAGAGT CTGTTTATTT 300
CTTGTTGACA CTAATCTTTG AGCATGAGTA GTTTAGTGAT TGTGAAACAG AAACTTCTGG 360
ATACAAAATC AGTCTCCTGG CTGTGACCCA ATCATCTTCG CAGTTCTGAT TACCTGTGAT 420
TAAGAAAATA AATAAGAACA CCCATTGGGG GAAGGCTTCC CTCCCCCGGG CACAGCAGCT 480
TTAAAACCGA AAGGGAAGTG GGTGCTGTGA GCAGCTCTGT TCAGGCCTAA GGCCACGCAT 540
GTGTGCCCCG TGGGGGAGAC ATGCACCAGC GAATCAGGAA ACAGTGGTGA CAGCCGTTCC 600
GGGAGGCTGA CTGGGGGTGC AGGGGTCACT TTTCTAATGT GGGTGGGTCT GTGTCCCCTG 660
CAGGAACGTG GCTGCAGCAA AGCCGGTCAG CCAGCGGTCA GCTCCAGCCC CTGTCCAGGC 720
CCTGTGGGTC CTGCTGACCA GGCTGCGGTT GTTCCCAAAC CAGTTCCCAG CCCCCGCTTG 780
CCCTACTTCC TCTCACACCA GCTCCTTCCA CCCCCTCACA CCCACCTGCA GGCTCCCAGC 840
CCAGGCTACT GACATCAATC ATGGCAATCG CTATTCCAGA GGTATACGCG GTGGGTGGGG 900
TCCGGTATCG CCTGCCATGC CTCACTCACC GGGCACCCAG ATAACCTGAG GCCAGGGAGC 960
AGCCACTCGC CCTGACCCAT GCTCCCCGGG CCCCTGAGGC ACCCAGGAGG ACCACCCGGC 1020
CGCTTCTGCT CAGAGCCCAG CACCCCCGAG TCTGTGAAGA GGTCACATCT GACCACGTTT 1080
CCAGGTGGCT GCCCAGGCGT GGGTTCATGG CCGCTTCCGG TTTCCTCCTC GAGCTGAACC 1140
ACACACCTGC TCTGTCCCGG GCTTTCTGGA GGGGTTTTCC GAAGTGAGAC TGTGGGCTCC 1200
CTCCAGGGCT GGGGGCAGGA GGACACACGG GGAAGGTGGG CAAGCAGCCC CAGGCTGAGG 1260
GAGGCCTCCC CTCTGCAGCG TTTGTTCATT CATTTGTTCA TCGCTAACAC TGTCTTGGGC 1320
ATCAGGGAAA ACAGGTGTCT CTGGTCCACA TGCAGAAGAG CCACCACCGT GGCACGACTG 1380
GATGACTCAG ACCCCGGGCG GGGGGTATGA TTTGGACACA GTCATTGTCC AGGGACACAA 1440
CTTTGCCTGG ACCAGAGCTT CTCACCCCCA GGCCATTTGA AACCCCAGGG GATACTCGAC 1500
AAAGTCCAGA GACATTTTGG GTTGTTCCTT TCCAGCCCCG GCGATGGTGG GGACGTGTCC 1560
ATGTCTGTGT CCCTCCGGTC ACTCTCTCTG GCCCTCTCCC TCCCTGGGGG CAGCTGCTCT 1620
CAGCCCTCCC TGCCCCCACA TCGCCATCCT GCCTGTCCTT CTGGGCCTGC ACGTTTGTTG 1680
TGTTTGGAAG GAGCCACCAA GGAGGAGGAT GTCAATGTGC AAGTTCTCAG GGAAGCAGGC 1740
CCCGCAGCCT CCGTCAGTGT CTTCCGTCCG CAGGAAGAAC CCAGGCCTGG GTGATTCATC 1800
GGGGCCTCAG GGCCGGGAGG CACTAAATCT TCTGCAGATG TGGTAAGATC CTATCACAGC 1860
AGAAAGGGAA GGGCTAGAGT CTCAGGGAAG GTTTTGCTAG GGAGACGGGC TTGGAGGGGG 1920
CTGAGGCTCA TGGGAGCTGC AAGGGTACAG GAGGGGAGGG GACCCCAGGG CAGGTGGATG 1980
GACACCTGGG TGGGTAAGAA AAGGGCCTCT CAGAGGGCAA GGGAGGGCCA GGGAGGGAGC 2040
AGTGAGCCCT GACTGACTGT ACAAGCTTAA CTGGCTGCCC TTGTCCTGCA GGTGGTGTGG 2100
GCTGTGTGGA TTTCGGATGT GGGCCCATAA CATAGCCACA CTGCTGCAAA GCAAGTGAGT 2160
CTGAGGCAAG AAGAAGGCCC AACCTTGGGA GGCTGACCTG GAGGGCAGGC AGAGGCAGGT 2220
GGTAAGGACC TGCCTTACCT GTTGAGGTGA CAGTGGGGGA CATATTGCAA GGAAGGAGGC 2280
CCTGGATCCT CAGGATGTGG ATGGTGGGTA GAAGGGTGAC AGCTAATGGA TGTCCACCTG 2340
CACAGATGCC CACCTGCATG AGTGCCCACC TGCATGAGTG CCCACTTGTA CCAATGTCCA 2400
CCTGTACAGA TGTCCACATG CAAATGCCCA TCTGCACTGA TATCCACCTG CACAGATGCC 2460
TACCTGCATG AATACCCACT TGCCTGAAAG CCCACCTGCA CCCATGTCCA CTGGCACAAA 2520
TGCCCACCTG CACCCGTGTC CACTGGCACA AATGCCCACC TGCACAGAAG CCCACCCACA 2580
CAAATGCCCA CCTGCAAAAA TGTCCGCCTG CACAGATGTC CACCTGCATG AATGCCCACC 2640
TGTGTCCACA TGCACGAATA CCCACCTGCA CAGATGCCCA CCTGCACGGA TGCCCACCTG 2700
TACAAAGGCC TACCTGCGTG AATGTCCACC TGCATGGATG CCCACCCGCA CGGATGCCCA 2760
CCTGCACAGT TATCCATCTG AACAGCCCTC TGGTGCCTCC TTTTGCTTGC ACATGTTCAA 2820