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

TagContent
EnhancerAtlas ID
HS064-02270 
Organism
Homo sapiens 
Tissue/cell
GM18507 
Coordinate
chr10:134234490-134237240 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
E2F6MA0471.1chr10:134235090-134235101CCTTCCCGCCC-6.62
Klf1MA0493.1chr10:134235338-134235349TGGGTGTGGCT-6.14
PAX6MA0069.1chr10:134236212-134236226TTCAAGCATGAATT+6.22
Twist2MA0633.1chr10:134237081-134237091AACATATGGT-6.02
ZNF263MA0528.1chr10:134234633-134234654GCTCCCTCCCCTTCCTGCCCC-6.7
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00873chr10:134226770-134236735Adrenal_Gland
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_24681chr10:134236793-134237997Colon_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_56893chr10:134236596-134237297VACO_400
SE_57427chr10:134233122-134236042VACO_503
SE_57946chr10:134234457-134236232VACO_9m
SE_60105chr10:134230766-134267420Ly4
SE_61428chr10:134196155-134334764Toledo
SE_65264chr10:134210665-134236634Pancreatic_islets
SE_65264chr10:134236908-134238178Pancreatic_islets
SE_68705chr10:134230320-134236371H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10134236652134237075
chr10134234707134235257
Enhancer Sequence
TCTCACACCC TGTGGGCCTT TTGCGTATTT CTTCCCGGGT GAGTTTTCTG GGCATTAACA 60
GATGTTTGCT CTGCAGACCT GGCCTTGTGT CACCCTGGAA CTCTGTGCCC AGCTCACCCT 120
TCCGTGGCTT CCTGTGGCCG GGGGCTCCCT CCCCTTCCTG CCCCAGGTCT GAGGTGCCAA 180
CGGCTGCCTG TGGCCAGGGG CATCTCCCCG TGGACACTGA GGGAGGAGCC GCGGCAGGGC 240
TGGGCTCTCC CGCTGGGCTC CCTGCACCCT GCGGCCCCGG CCCCAGCCCC ACCCCCAGCC 300
ATGGGAAGGG TGCACTCCGG AGAGGCCGAC GCAGATGGGG CCCTGCCCCT GGCCTGAGCG 360
TGGCCGTCAT CTGCTCAGGA GGGTTAAGCT CCTTTGTGCC CCAAGGAGCT TCAAGCCGAT 420
CAATACCCGG CTGGAAGTAG GGGGCTGCAG CTGGGGGGGC CCCACCGCCC TGACCCCAGA 480
TGGACTTCCT GCTCCCTGCC CAGCTTCTCT GCGGGGGGAG GTCAGGTCAG TGGGCCTCCT 540
GCTTGGCCTT TGGGGCCACC GCCCCTGGGC TCCAGCTGAG GCTGTCCCAG GGCCGGTCTC 600
CCTTCCCGCC CCCACCCTAC AGAGGCGGCC TCACCAGCCA GCCTCTGCCC CAGCAGAGTT 660
ATTTTTAGCC CCAGCCCCGC CTGCTGCTAC CACGGGCCTT TTCTCCGCAG AGAGAGGCGG 720
GTGAGGCCTG AGGGCCTCAC CCAGGGCAGC CAGTTCCCCA ACCACGAAGG GAGGCAGGAG 780
AGCTTCCCTG TGCGGGCAGG CGTCGCTGAC CCTCCAAGGG GCAGAGCAGT GGGGGCTTCC 840
TTCCTTCCTG GGTGTGGCTG GGGGGAGGGG GCTGAAGGCC TGGAGCCGGA GGGGCTTGCC 900
CTAGAGCCCC ATAGCCAGGC AGGGGTCAGT GTCCACAGCT GGAGGGGCTG GAGAGGTGAG 960
AGAGATGGTC CCAAGGGAGC TGGGAGGCCC AGGAGTGGGC CCAGTGCTCA ACCCGCTGCC 1020
AGGCAGGGAC AAGACCTGAG AGATGAGAGG GCGGCGGGGG TGACCCTCGG AGGGCAGAGG 1080
GCGCCAGGAC GGAGAGATGA ACGGGGCAGT GGGGTGACCC ATGGAGACCC ACAGAGAGCA 1140
GAGGGGCACC AGGATGGGGA GACGGAGGCC AGTGGGGGCT GAGGGGTCCC GGGGGAGGAC 1200
TGTAAGGAGC CACATAGTGG CTGCGGTCGG CGTGGCTGGG AGACAGGGGT CCAGGAAGCC 1260
CACTGGAAGC TGCCGCCCCG GCTGTAGCTG CAGGGCTCTC TGTGGGAGCC GGGAGCTGGG 1320
TGCAGAGCTG CGTCGAGGCT GCCTGAGGCC TGGCAGCCCA GCAGGAGGGG ACTTACCCCC 1380
ACCCCCCCAC GGAGGAGAAG GCTCTGGGGC CTGCTGGGTG CAGACGCAGC TGGGATCTGC 1440
TTTGGGGAAG AAAACCTAGG CAGGTCACCG AGGCTCTGCC CAAGCCAACG CCTGTCACCT 1500
GTCACCGAGG TGTGGGTGTC TGTCCTCCTC CCAGCCGTCC ATCCCCCTCC CTCCTGGCCC 1560
CGCTCCAGCC CGCAGCCCCC ATGGGAGCCC GAGAGAGGAC AGTCTCAGCA GGTGGCACAG 1620
ACAGATGCGG ACTCCTCACT GCAGGTCACA AGGCATGTTT TCAGAGACCA GCTGCGGTGA 1680
AGATCATCCA GCCCTTGGGC CCCTGATCCG TTTGGATACA GTTTCAAGCA TGAATTTCTC 1740
CTTTGGTGGT TTGCTACAAA GAGAAGAGTT CTCATGATTT CTTTGGGGTG TTCATCCTAT 1800
GATTTTGGGG TGAGGATTCG TGACAGAGAC AAGCAACAGG AGTCCAGGAA GCCCTCGGGG 1860
GAGACGGGAA ACAAGTCTTT TTGAAAAAAC AGCTTTCTTT GAGACGTAGC TCACATATCA 1920
TATGATCCCT CCCCTTCCAG TGGACACGTC CATGGCTTTC AGCGTGTTTA TAGATGGGCA 1980
ACATCCCCAC GGGCCCTTTT AGAACATTCG CTTCACCTCA GAAAGAAACC CCACAGCTTT 2040
TAGCCATCAC CCTCCTCCCC AGGCCTAAGC AGTCCCTCAT CTGCTTCCGT CTCTGGGGAC 2100
TTCCCTGTTC TGCGTTCTGT GTGACATGTG GTTGTGTGTG ATTTATGATT GTGTGTAACA 2160
TGCGTTCCAT TTCATCCATG TGACATGCGG TTGTGTGGGA GATATGATTG TGTGTAACAT 2220
GCGTTCTGTA TGATGTGCGG TTGTGTGTGA GATACAGTTG TGTGTAACAC ACATTCTGTA 2280
TGACGTGCAG TTATGTGTAA GATACGGTGT GTAACACATG TTCCATGTGA CATGTGGTTT 2340
GTGTGATTTA TGATTGTAAC ATGCATTCCA TGTGGTCCGT GTGACGTGGT TGTGTGTGAT 2400
ACACCATTGC ATGTAACGTG TTCCGTGTGA TGTGTGGTTG TGTGTGACAC ACCGTTGTGT 2460
GTAGCATGTG TTCTGGCAGG CGGTCGTGTG TGGCTTCCTT CGCCGAGCAC AGTGCTTTCA 2520
CGATGCCCCC GTGTTGGCGC GTGCCTGTGC CCCATTCCTT TCTATGCTGA ATGATGCTCC 2580
CCATGTGGGT GAACATATGG TGTTTGTCCA TCTGTCAGTC TGTGGACATG TGAGCTGTCT 2640
CTGCCTTTTG GCTGCTGTGC ACAAAGCTGC TGTGAGCTTT CCTGCAGTCT CTGTGTGGCT 2700
GTGTGTGTGT GTGGCTGTGT GTGTGGCTGT GTGTGTGTGG CTGTGTGTGT 2750