EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-04049 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr10:134233240-134236700 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10781573chr10134233608hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr10:134235090-134235101CCTTCCCGCCC-6.62
Klf1MA0493.1chr10:134235338-134235349TGGGTGTGGCT-6.14
PAX6MA0069.1chr10:134236212-134236226TTCAAGCATGAATT+6.22
ZNF263MA0528.1chr10:134233872-134233893TGTTCTTCATCTTCCTCCTCT-6.11
ZNF263MA0528.1chr10:134234633-134234654GCTCCCTCCCCTTCCTGCCCC-6.7
ZNF263MA0528.1chr10:134233845-134233866CCTTCTTTCTCTTCTTCCTCT-6.86
ZNF263MA0528.1chr10:134233848-134233869TCTTTCTCTTCTTCCTCTTCC-6.86
ZNF263MA0528.1chr10:134233851-134233872TTCTCTTCTTCCTCTTCCTCT-6.97
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00873chr10:134226770-134236735Adrenal_Gland
SE_02964chr10:134233042-134233655Bladder
SE_02964chr10:134233682-134236060Bladder
SE_04410chr10:134233156-134238501Brain_Anterior_Caudate
SE_09804chr10:134228334-134237697CD14
SE_10426chr10:134229819-134237452CD19_Primary
SE_11568chr10:134228105-134238193CD20
SE_23061chr10:134228659-134236350Colon_Crypt_1
SE_23725chr10:134229390-134236228Colon_Crypt_2
SE_24681chr10:134229263-134236759Colon_Crypt_3
SE_26753chr10:134230541-134237300Esophagus
SE_28153chr10:134231057-134236765Fetal_Intestine
SE_29112chr10:134231073-134236603Fetal_Intestine_Large
SE_31406chr10:134229991-134236773Gastric
SE_33290chr10:134234813-134235602H1
SE_34405chr10:134231475-134236275HCT-116
SE_41567chr10:134233089-134236216LNCaP
SE_42252chr10:134219499-134237674Lung
SE_47467chr10:134231344-134236211Pancreas
SE_50143chr10:134230102-134237596Sigmoid_Colon
SE_53287chr10:134219205-134237202Spleen
SE_56893chr10:134230770-134236362VACO_400
SE_57427chr10:134233122-134236042VACO_503
SE_57946chr10:134233437-134234418VACO_9m
SE_57946chr10:134234457-134236232VACO_9m
SE_60105chr10:134230766-134267420Ly4
SE_61428chr10:134196155-134334764Toledo
SE_65264chr10:134210665-134236634Pancreatic_islets
SE_68705chr10:134230320-134236371H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10134233972134236600
chr10134234707134235257
Enhancer Sequence
GGGGCTGCCC GGAGCTGGTC CTGGGCCTCT CTTGCTCTGG GTCTCCCCTG CTCTGGGTCC 60
AGCCTCCCAA GCACCCCACC TGGCAAGACT TCCTCGCTCA GAACAGAGCC AACCCTGGCT 120
GTCTTCCCAG GGTTTGTCGT GGAGAGGGCT CTGGCCCTTT AGCCTTCCAA GGAGCTTTCG 180
GGGTTGGGGT ACGTTTGTGA CCCCAGTAGC CGCTGTGCTG GGGGCCCAGG GCAACTCCTC 240
CGGGAGCAGG GAAGGCACTG CTGGCACCAC CAGCCCCGCA GGGTCACCAG CATCCCGTCT 300
CCACCAGGGC TGCTGCTGTC CCTCCTCTGC TGAGGCCAGC TGTTACCGTG TTCGACATGG 360
ACCAGGCCGT GTGGGAGGAC ACGGGGTGGC AGGTGCAGGG AGCACGGTCT GTTTTCTGTC 420
ACTCTCTGGT CCCAGCCTGA GCCCCAATCC CTACCTCTGA GGGTCACACT TCCAACCCAC 480
CCCAGACAGA GCTGGAAGCA GGGGCTGGCA TGGGCGCTGG GGTAGACGCA GGGGTTGTCG 540
TGGCCTGGCG TGGAAGAGCT GGGCTGGACG CAGTGGGTGG CGTGGCCTGG GGTGCTGCTC 600
TCCAGCCTTC TTTCTCTTCT TCCTCTTCCT CTTGTTCTTC ATCTTCCTCC TCTTGCTGCA 660
GATCCTCCCC CAGGTGGCTC CATTTCTGCT GGTCCCATCT CCCGGAGGCC CTGCCCACAA 720
CCCCCTGCCC GCCATCTAGG GGGACCCTGG CGTGGTCCAG GAGAGGGAGT CAAGGCCTGT 780
GTGGGGCTCC TGGGGCTGGA GTCCTGGTCT GCCTTCTGGG GACAGAGACT AGGTCGCCCT 840
GGGCTCCAGC TCTGTGGCCT GGCTGTGTGG GCTGGGCCAG GGCCTCTGCG TCACCTCCTT 900
GCCTGGGCTT CTCACAGTGC AAGCCCCGCA GCCTAGGCCC TGCTGGGTGG TGGTGGGATG 960
GCTGGGGAGG GGCAAGAGCA GGTGAGGAGT CCTCACTGGG GGTGCATACT TTGCATTACA 1020
GCTGGGGAGG CTGAGACCCG GGGGGCCACA GCTGGTTCCT GGACTCCAAA GCCCAGGACC 1080
CTTCCAAATC CTGCCTGGAC GGCACCGTGG CCAGGACCCC AGCCAGCACT TCCCTTTTCT 1140
GCGAGGGTTT TCTGTTTCTT TGATTATAAA ATAACCCCTG TTGGTGGGGG GAAAAAATTA 1200
GCAAAATAAA GAAAAGCAAA AAAAAAAAAG AAAATTAGAA TCTCCCGCAG TCTCACACCC 1260
TGTGGGCCTT TTGCGTATTT CTTCCCGGGT GAGTTTTCTG GGCATTAACA GATGTTTGCT 1320
CTGCAGACCT GGCCTTGTGT CACCCTGGAA CTCTGTGCCC AGCTCACCCT TCCGTGGCTT 1380
CCTGTGGCCG GGGGCTCCCT CCCCTTCCTG CCCCAGGTCT GAGGTGCCAA CGGCTGCCTG 1440
TGGCCAGGGG CATCTCCCCG TGGACACTGA GGGAGGAGCC GCGGCAGGGC TGGGCTCTCC 1500
CGCTGGGCTC CCTGCACCCT GCGGCCCCGG CCCCAGCCCC ACCCCCAGCC ATGGGAAGGG 1560
TGCACTCCGG AGAGGCCGAC GCAGATGGGG CCCTGCCCCT GGCCTGAGCG TGGCCGTCAT 1620
CTGCTCAGGA GGGTTAAGCT CCTTTGTGCC CCAAGGAGCT TCAAGCCGAT CAATACCCGG 1680
CTGGAAGTAG GGGGCTGCAG CTGGGGGGGC CCCACCGCCC TGACCCCAGA TGGACTTCCT 1740
GCTCCCTGCC CAGCTTCTCT GCGGGGGGAG GTCAGGTCAG TGGGCCTCCT GCTTGGCCTT 1800
TGGGGCCACC GCCCCTGGGC TCCAGCTGAG GCTGTCCCAG GGCCGGTCTC CCTTCCCGCC 1860
CCCACCCTAC AGAGGCGGCC TCACCAGCCA GCCTCTGCCC CAGCAGAGTT ATTTTTAGCC 1920
CCAGCCCCGC CTGCTGCTAC CACGGGCCTT TTCTCCGCAG AGAGAGGCGG GTGAGGCCTG 1980
AGGGCCTCAC CCAGGGCAGC CAGTTCCCCA ACCACGAAGG GAGGCAGGAG AGCTTCCCTG 2040
TGCGGGCAGG CGTCGCTGAC CCTCCAAGGG GCAGAGCAGT GGGGGCTTCC TTCCTTCCTG 2100
GGTGTGGCTG GGGGGAGGGG GCTGAAGGCC TGGAGCCGGA GGGGCTTGCC CTAGAGCCCC 2160
ATAGCCAGGC AGGGGTCAGT GTCCACAGCT GGAGGGGCTG GAGAGGTGAG AGAGATGGTC 2220
CCAAGGGAGC TGGGAGGCCC AGGAGTGGGC CCAGTGCTCA ACCCGCTGCC AGGCAGGGAC 2280
AAGACCTGAG AGATGAGAGG GCGGCGGGGG TGACCCTCGG AGGGCAGAGG GCGCCAGGAC 2340
GGAGAGATGA ACGGGGCAGT GGGGTGACCC ATGGAGACCC ACAGAGAGCA GAGGGGCACC 2400
AGGATGGGGA GACGGAGGCC AGTGGGGGCT GAGGGGTCCC GGGGGAGGAC TGTAAGGAGC 2460
CACATAGTGG CTGCGGTCGG CGTGGCTGGG AGACAGGGGT CCAGGAAGCC CACTGGAAGC 2520
TGCCGCCCCG GCTGTAGCTG CAGGGCTCTC TGTGGGAGCC GGGAGCTGGG TGCAGAGCTG 2580
CGTCGAGGCT GCCTGAGGCC TGGCAGCCCA GCAGGAGGGG ACTTACCCCC ACCCCCCCAC 2640
GGAGGAGAAG GCTCTGGGGC CTGCTGGGTG CAGACGCAGC TGGGATCTGC TTTGGGGAAG 2700
AAAACCTAGG CAGGTCACCG AGGCTCTGCC CAAGCCAACG CCTGTCACCT GTCACCGAGG 2760
TGTGGGTGTC TGTCCTCCTC CCAGCCGTCC ATCCCCCTCC CTCCTGGCCC CGCTCCAGCC 2820
CGCAGCCCCC ATGGGAGCCC GAGAGAGGAC AGTCTCAGCA GGTGGCACAG ACAGATGCGG 2880
ACTCCTCACT GCAGGTCACA AGGCATGTTT TCAGAGACCA GCTGCGGTGA AGATCATCCA 2940
GCCCTTGGGC CCCTGATCCG TTTGGATACA GTTTCAAGCA TGAATTTCTC CTTTGGTGGT 3000
TTGCTACAAA GAGAAGAGTT CTCATGATTT CTTTGGGGTG TTCATCCTAT GATTTTGGGG 3060
TGAGGATTCG TGACAGAGAC AAGCAACAGG AGTCCAGGAA GCCCTCGGGG GAGACGGGAA 3120
ACAAGTCTTT TTGAAAAAAC AGCTTTCTTT GAGACGTAGC TCACATATCA TATGATCCCT 3180
CCCCTTCCAG TGGACACGTC CATGGCTTTC AGCGTGTTTA TAGATGGGCA ACATCCCCAC 3240
GGGCCCTTTT AGAACATTCG CTTCACCTCA GAAAGAAACC CCACAGCTTT TAGCCATCAC 3300
CCTCCTCCCC AGGCCTAAGC AGTCCCTCAT CTGCTTCCGT CTCTGGGGAC TTCCCTGTTC 3360
TGCGTTCTGT GTGACATGTG GTTGTGTGTG ATTTATGATT GTGTGTAACA TGCGTTCCAT 3420
TTCATCCATG TGACATGCGG TTGTGTGGGA GATATGATTG 3460