EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS171-00144 
Organism
Homo sapiens 
Tissue/cell
SEM 
Coordinate
chr10:134233550-134237070 
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_02964chr10:134233682-134236060Bladder
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_56893chr10:134236596-134237297VACO_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
TGCTGCTGTC CCTCCTCTGC TGAGGCCAGC TGTTACCGTG TTCGACATGG ACCAGGCCGT 60
GTGGGAGGAC ACGGGGTGGC AGGTGCAGGG AGCACGGTCT GTTTTCTGTC ACTCTCTGGT 120
CCCAGCCTGA GCCCCAATCC CTACCTCTGA GGGTCACACT TCCAACCCAC CCCAGACAGA 180
GCTGGAAGCA GGGGCTGGCA TGGGCGCTGG GGTAGACGCA GGGGTTGTCG TGGCCTGGCG 240
TGGAAGAGCT GGGCTGGACG CAGTGGGTGG CGTGGCCTGG GGTGCTGCTC TCCAGCCTTC 300
TTTCTCTTCT TCCTCTTCCT CTTGTTCTTC ATCTTCCTCC TCTTGCTGCA GATCCTCCCC 360
CAGGTGGCTC CATTTCTGCT GGTCCCATCT CCCGGAGGCC CTGCCCACAA CCCCCTGCCC 420
GCCATCTAGG GGGACCCTGG CGTGGTCCAG GAGAGGGAGT CAAGGCCTGT GTGGGGCTCC 480
TGGGGCTGGA GTCCTGGTCT GCCTTCTGGG GACAGAGACT AGGTCGCCCT GGGCTCCAGC 540
TCTGTGGCCT GGCTGTGTGG GCTGGGCCAG GGCCTCTGCG TCACCTCCTT GCCTGGGCTT 600
CTCACAGTGC AAGCCCCGCA GCCTAGGCCC TGCTGGGTGG TGGTGGGATG GCTGGGGAGG 660
GGCAAGAGCA GGTGAGGAGT CCTCACTGGG GGTGCATACT TTGCATTACA GCTGGGGAGG 720
CTGAGACCCG GGGGGCCACA GCTGGTTCCT GGACTCCAAA GCCCAGGACC CTTCCAAATC 780
CTGCCTGGAC GGCACCGTGG CCAGGACCCC AGCCAGCACT TCCCTTTTCT GCGAGGGTTT 840
TCTGTTTCTT TGATTATAAA ATAACCCCTG TTGGTGGGGG GAAAAAATTA GCAAAATAAA 900
GAAAAGCAAA AAAAAAAAAG AAAATTAGAA TCTCCCGCAG TCTCACACCC TGTGGGCCTT 960
TTGCGTATTT CTTCCCGGGT GAGTTTTCTG GGCATTAACA GATGTTTGCT CTGCAGACCT 1020
GGCCTTGTGT CACCCTGGAA CTCTGTGCCC AGCTCACCCT TCCGTGGCTT CCTGTGGCCG 1080
GGGGCTCCCT CCCCTTCCTG CCCCAGGTCT GAGGTGCCAA CGGCTGCCTG TGGCCAGGGG 1140
CATCTCCCCG TGGACACTGA GGGAGGAGCC GCGGCAGGGC TGGGCTCTCC CGCTGGGCTC 1200
CCTGCACCCT GCGGCCCCGG CCCCAGCCCC ACCCCCAGCC ATGGGAAGGG TGCACTCCGG 1260
AGAGGCCGAC GCAGATGGGG CCCTGCCCCT GGCCTGAGCG TGGCCGTCAT CTGCTCAGGA 1320
GGGTTAAGCT CCTTTGTGCC CCAAGGAGCT TCAAGCCGAT CAATACCCGG CTGGAAGTAG 1380
GGGGCTGCAG CTGGGGGGGC CCCACCGCCC TGACCCCAGA TGGACTTCCT GCTCCCTGCC 1440
CAGCTTCTCT GCGGGGGGAG GTCAGGTCAG TGGGCCTCCT GCTTGGCCTT TGGGGCCACC 1500
GCCCCTGGGC TCCAGCTGAG GCTGTCCCAG GGCCGGTCTC CCTTCCCGCC CCCACCCTAC 1560
AGAGGCGGCC TCACCAGCCA GCCTCTGCCC CAGCAGAGTT ATTTTTAGCC CCAGCCCCGC 1620
CTGCTGCTAC CACGGGCCTT TTCTCCGCAG AGAGAGGCGG GTGAGGCCTG AGGGCCTCAC 1680
CCAGGGCAGC CAGTTCCCCA ACCACGAAGG GAGGCAGGAG AGCTTCCCTG TGCGGGCAGG 1740
CGTCGCTGAC CCTCCAAGGG GCAGAGCAGT GGGGGCTTCC TTCCTTCCTG GGTGTGGCTG 1800
GGGGGAGGGG GCTGAAGGCC TGGAGCCGGA GGGGCTTGCC CTAGAGCCCC ATAGCCAGGC 1860
AGGGGTCAGT GTCCACAGCT GGAGGGGCTG GAGAGGTGAG AGAGATGGTC CCAAGGGAGC 1920
TGGGAGGCCC AGGAGTGGGC CCAGTGCTCA ACCCGCTGCC AGGCAGGGAC AAGACCTGAG 1980
AGATGAGAGG GCGGCGGGGG TGACCCTCGG AGGGCAGAGG GCGCCAGGAC GGAGAGATGA 2040
ACGGGGCAGT GGGGTGACCC ATGGAGACCC ACAGAGAGCA GAGGGGCACC AGGATGGGGA 2100
GACGGAGGCC AGTGGGGGCT GAGGGGTCCC GGGGGAGGAC TGTAAGGAGC CACATAGTGG 2160
CTGCGGTCGG CGTGGCTGGG AGACAGGGGT CCAGGAAGCC CACTGGAAGC TGCCGCCCCG 2220
GCTGTAGCTG CAGGGCTCTC TGTGGGAGCC GGGAGCTGGG TGCAGAGCTG CGTCGAGGCT 2280
GCCTGAGGCC TGGCAGCCCA GCAGGAGGGG ACTTACCCCC ACCCCCCCAC GGAGGAGAAG 2340
GCTCTGGGGC CTGCTGGGTG CAGACGCAGC TGGGATCTGC TTTGGGGAAG AAAACCTAGG 2400
CAGGTCACCG AGGCTCTGCC CAAGCCAACG CCTGTCACCT GTCACCGAGG TGTGGGTGTC 2460
TGTCCTCCTC CCAGCCGTCC ATCCCCCTCC CTCCTGGCCC CGCTCCAGCC CGCAGCCCCC 2520
ATGGGAGCCC GAGAGAGGAC AGTCTCAGCA GGTGGCACAG ACAGATGCGG ACTCCTCACT 2580
GCAGGTCACA AGGCATGTTT TCAGAGACCA GCTGCGGTGA AGATCATCCA GCCCTTGGGC 2640
CCCTGATCCG TTTGGATACA GTTTCAAGCA TGAATTTCTC CTTTGGTGGT TTGCTACAAA 2700
GAGAAGAGTT CTCATGATTT CTTTGGGGTG TTCATCCTAT GATTTTGGGG TGAGGATTCG 2760
TGACAGAGAC AAGCAACAGG AGTCCAGGAA GCCCTCGGGG GAGACGGGAA ACAAGTCTTT 2820
TTGAAAAAAC AGCTTTCTTT GAGACGTAGC TCACATATCA TATGATCCCT CCCCTTCCAG 2880
TGGACACGTC CATGGCTTTC AGCGTGTTTA TAGATGGGCA ACATCCCCAC GGGCCCTTTT 2940
AGAACATTCG CTTCACCTCA GAAAGAAACC CCACAGCTTT TAGCCATCAC CCTCCTCCCC 3000
AGGCCTAAGC AGTCCCTCAT CTGCTTCCGT CTCTGGGGAC TTCCCTGTTC TGCGTTCTGT 3060
GTGACATGTG GTTGTGTGTG ATTTATGATT GTGTGTAACA TGCGTTCCAT TTCATCCATG 3120
TGACATGCGG TTGTGTGGGA GATATGATTG TGTGTAACAT GCGTTCTGTA TGATGTGCGG 3180
TTGTGTGTGA GATACAGTTG TGTGTAACAC ACATTCTGTA TGACGTGCAG TTATGTGTAA 3240
GATACGGTGT GTAACACATG TTCCATGTGA CATGTGGTTT GTGTGATTTA TGATTGTAAC 3300
ATGCATTCCA TGTGGTCCGT GTGACGTGGT TGTGTGTGAT ACACCATTGC ATGTAACGTG 3360
TTCCGTGTGA TGTGTGGTTG TGTGTGACAC ACCGTTGTGT GTAGCATGTG TTCTGGCAGG 3420
CGGTCGTGTG TGGCTTCCTT CGCCGAGCAC AGTGCTTTCA CGATGCCCCC GTGTTGGCGC 3480
GTGCCTGTGC CCCATTCCTT TCTATGCTGA ATGATGCTCC 3520