EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-26221 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr21:45626050-45629080 
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
ATTTGGGGTC CGCAGAGGCA AACCACAGGA GGACGGAGTC GGAGACTGGA GCACCGCGGC 60
CTTGATCGGG GGACACCAGG GCTGCCGGCT GTGCCAGAAG GGGCTGAGGC TGGACCGGAT 120
TCTCTCCGAG TTCCCAGAAG GAGCCAGTCC TGCCGACGCC TTGATGCTGG ACTCTGGCCT 180
CCAGAAATGT GCGAGGACAA ACATCTGCGG TTTCTAGGCC CCGCCTGTGG TCCTCTGTTG 240
CAGCAGCCTG GACAGTCTGG ACTGCCTGGA CAGCATGCAG ATGGGCTCTG CCCGCGGCTG 300
CCCACGAGTT CCCACCGCCC GCCCGTCCGT GGGAGAGCCA GTCCTCGTAT GTGAAGCGTA 360
CCTGTATCCC TTTACTCCGC GTACACAGGT GCCTTTGTCA CTTCTCCTTT GACCTGGCTG 420
GCACATCTTA CCGGTTTCTG CGCTAACAAT GAGTTGAAGG AAATCTTGAA CGCGCGTTCA 480
TTTTATATCG GTATCAGAGT CTGTTTATTT CTTGTTGACA CTAATCTTTG AGCATGAGTA 540
GTTTAGTGAT TGTGAAACAG AAACTTCTGG ATACAAAATC AGTCTCCTGG CTGTGACCCA 600
ATCATCTTCG CAGTTCTGAT TACCTGTGAT TAAGAAAATA AATAAGAACA CCCATTGGGG 660
GAAGGCTTCC CTCCCCCGGG CACAGCAGCT TTAAAACCGA AAGGGAAGTG GGTGCTGTGA 720
GCAGCTCTGT TCAGGCCTAA GGCCACGCAT GTGTGCCCCG TGGGGGAGAC ATGCACCAGC 780
GAATCAGGAA ACAGTGGTGA CAGCCGTTCC GGGAGGCTGA CTGGGGGTGC AGGGGTCACT 840
TTTCTAATGT GGGTGGGTCT GTGTCCCCTG CAGGAACGTG GCTGCAGCAA AGCCGGTCAG 900
CCAGCGGTCA GCTCCAGCCC CTGTCCAGGC CCTGTGGGTC CTGCTGACCA GGCTGCGGTT 960
GTTCCCAAAC CAGTTCCCAG CCCCCGCTTG CCCTACTTCC TCTCACACCA GCTCCTTCCA 1020
CCCCCTCACA CCCACCTGCA GGCTCCCAGC CCAGGCTACT GACATCAATC ATGGCAATCG 1080
CTATTCCAGA GGTATACGCG GTGGGTGGGG TCCGGTATCG CCTGCCATGC CTCACTCACC 1140
GGGCACCCAG ATAACCTGAG GCCAGGGAGC AGCCACTCGC CCTGACCCAT GCTCCCCGGG 1200
CCCCTGAGGC ACCCAGGAGG ACCACCCGGC CGCTTCTGCT CAGAGCCCAG CACCCCCGAG 1260
TCTGTGAAGA GGTCACATCT GACCACGTTT CCAGGTGGCT GCCCAGGCGT GGGTTCATGG 1320
CCGCTTCCGG TTTCCTCCTC GAGCTGAACC ACACACCTGC TCTGTCCCGG GCTTTCTGGA 1380
GGGGTTTTCC GAAGTGAGAC TGTGGGCTCC CTCCAGGGCT GGGGGCAGGA GGACACACGG 1440
GGAAGGTGGG CAAGCAGCCC CAGGCTGAGG GAGGCCTCCC CTCTGCAGCG TTTGTTCATT 1500
CATTTGTTCA TCGCTAACAC TGTCTTGGGC ATCAGGGAAA ACAGGTGTCT CTGGTCCACA 1560
TGCAGAAGAG CCACCACCGT GGCACGACTG GATGACTCAG ACCCCGGGCG GGGGGTATGA 1620
TTTGGACACA GTCATTGTCC AGGGACACAA CTTTGCCTGG ACCAGAGCTT CTCACCCCCA 1680
GGCCATTTGA AACCCCAGGG GATACTCGAC AAAGTCCAGA GACATTTTGG GTTGTTCCTT 1740
TCCAGCCCCG GCGATGGTGG GGACGTGTCC ATGTCTGTGT CCCTCCGGTC ACTCTCTCTG 1800
GCCCTCTCCC TCCCTGGGGG CAGCTGCTCT CAGCCCTCCC TGCCCCCACA TCGCCATCCT 1860
GCCTGTCCTT CTGGGCCTGC ACGTTTGTTG TGTTTGGAAG GAGCCACCAA GGAGGAGGAT 1920
GTCAATGTGC AAGTTCTCAG GGAAGCAGGC CCCGCAGCCT CCGTCAGTGT CTTCCGTCCG 1980
CAGGAAGAAC CCAGGCCTGG GTGATTCATC GGGGCCTCAG GGCCGGGAGG CACTAAATCT 2040
TCTGCAGATG TGGTAAGATC CTATCACAGC AGAAAGGGAA GGGCTAGAGT CTCAGGGAAG 2100
GTTTTGCTAG GGAGACGGGC TTGGAGGGGG CTGAGGCTCA TGGGAGCTGC AAGGGTACAG 2160
GAGGGGAGGG GACCCCAGGG CAGGTGGATG GACACCTGGG TGGGTAAGAA AAGGGCCTCT 2220
CAGAGGGCAA GGGAGGGCCA GGGAGGGAGC AGTGAGCCCT GACTGACTGT ACAAGCTTAA 2280
CTGGCTGCCC TTGTCCTGCA GGTGGTGTGG GCTGTGTGGA TTTCGGATGT GGGCCCATAA 2340
CATAGCCACA CTGCTGCAAA GCAAGTGAGT CTGAGGCAAG AAGAAGGCCC AACCTTGGGA 2400
GGCTGACCTG GAGGGCAGGC AGAGGCAGGT GGTAAGGACC TGCCTTACCT GTTGAGGTGA 2460
CAGTGGGGGA CATATTGCAA GGAAGGAGGC CCTGGATCCT CAGGATGTGG ATGGTGGGTA 2520
GAAGGGTGAC AGCTAATGGA TGTCCACCTG CACAGATGCC CACCTGCATG AGTGCCCACC 2580
TGCATGAGTG CCCACTTGTA CCAATGTCCA CCTGTACAGA TGTCCACATG CAAATGCCCA 2640
TCTGCACTGA TATCCACCTG CACAGATGCC TACCTGCATG AATACCCACT TGCCTGAAAG 2700
CCCACCTGCA CCCATGTCCA CTGGCACAAA TGCCCACCTG CACCCGTGTC CACTGGCACA 2760
AATGCCCACC TGCACAGAAG CCCACCCACA CAAATGCCCA CCTGCAAAAA TGTCCGCCTG 2820
CACAGATGTC CACCTGCATG AATGCCCACC TGTGTCCACA TGCACGAATA CCCACCTGCA 2880
CAGATGCCCA CCTGCACGGA TGCCCACCTG TACAAAGGCC TACCTGCGTG AATGTCCACC 2940
TGCATGGATG CCCACCCGCA CGGATGCCCA CCTGCACAGT TATCCATCTG AACAGCCCTC 3000
TGGTGCCTCC TTTTGCTTGC ACATGTTCAA 3030