EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-04921 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr10:134231470-134234320 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10781573chr10134233608hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr10:134233872-134233893TGTTCTTCATCTTCCTCCTCT-6.11
ZNF263MA0528.1chr10:134232195-134232216CCTTCCCCTCCTCCCTCCCCG-6.19
ZNF263MA0528.1chr10:134231878-134231899GGGGGAGGGGTCGGGGGAGGG+6.69
ZNF263MA0528.1chr10:134233845-134233866CCTTCTTTCTCTTCTTCCTCT-6.86
ZNF263MA0528.1chr10:134233848-134233869TCTTTCTCTTCTTCCTCTTCC-6.86
ZNF263MA0528.1chr10:134233851-134233872TTCTCTTCTTCCTCTTCCTCT-6.97
ZNF263MA0528.1chr10:134232191-134232212CTCCCCTTCCCCTCCTCCCTC-7.97
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00873chr10:134226770-134236735Adrenal_Gland
SE_02964chr10:134231826-134233017Bladder
SE_02964chr10:134233042-134233655Bladder
SE_02964chr10:134233682-134236060Bladder
SE_04410chr10:134231065-134232866Brain_Anterior_Caudate
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_33290chr10:134231995-134232554H1
SE_34405chr10:134231475-134236275HCT-116
SE_41567chr10:134228546-134232988LNCaP
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_57427chr10:134231383-134233121VACO_503
SE_57427chr10:134233122-134236042VACO_503
SE_57946chr10:134231417-134233028VACO_9m
SE_57946chr10:134233437-134234418VACO_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: 1             
ChromosomeStartEnd
chr10134233193134233800
Enhancer Sequence
TCCCTGTCGG GGCTGACGGG GCCTGAGTCC CCTGGGCACT GCTGGGCGGG GCCCATGTCG 60
TACGGGTTGG GGTGACGCCG CCACCGGCTG CATCTCGCTG CCTCCAGGTG GGGGGACGCT 120
GGTCACCGCC CTGAGCCCCA GGAGGGCTGT GGGCTGAGTC CCCATCTCCA GGCCTCCCTG 180
CTGGCTTTCC AGTGGACGCT GGGATTTCCT GGAGAGGCAG TGCTCTGCAC GCGGGGAGCT 240
TTGTTCTTTG TTTCCTGGAG TGACTCCTCT CATCCCTTGT TTCTTGATTT GCTCATTCAG 300
AACCAAGGGA GATCTCAGAG ATGACGATGG TGGCTTTGCT TGTTCCTGGT TTTGCTAGAA 360
CATTCTGTGC TCTAAAGGCA TCGCTGCCCT CAGCAAGGAT CGTCTGGCGG GGGAGGGGTC 420
GGGGGAGGGC AGCAGCATAC ACCTGGAGGG TCCTCTCCAG GGCACATGAG GGAACAACCC 480
TCATGGTTTC CTATGGTTCT GGACCTGACT TGCGAGGAGG GGCATGGTTT TCAAACTGGT 540
TTGTAGCAGC AGAGCCCTTT TCTCCAACAA AATCACCCAG AATCACTTCC TCCCGGAGGG 600
GCTGGGCTCA TCCTCCTGAA GCCCTCCAGG CCCAAGAGTC CTGGGAAGCC TTTGAAAATC 660
CAGGGAGGGG CTCGCATGAG CCCAGGAGAG CAGAGCCAGG ACTTGAGAGG AATGAGAGCA 720
GCTCCCCTTC CCCTCCTCCC TCCCCGGCCC TGCCCACGTG GGTGCAGCAG AGTCAGGGCC 780
CTGGCCCTTG GGGCTGGGCA TCTCATCCCT CTGAGCTCCG GTGCCCAGGG GCTGCCCCTG 840
CCTGATCTGC TGCTCGGGGT GACTCCCCCT GCCGCACACC CCACTTTGCA CCCAGGACCT 900
CCTACTGACT AGGGTTGGCT CCCCTTTACG AAGGAAGGCC TTCGTAAAGC TTGGCACTGC 960
TTCAAGAAAT GTGTGTGTCC AATGGAAGGA GCAGGCCTCA CCCCTGGGAC AAAATATGCG 1020
TGCAGCCCTG GGCACATTCA CTCCCAGCTG CCCAGCCTGC AACTAGAGCT CAGCCACTGC 1080
AGGTGACAGC AACGGGACCC GCCTTTGAGC CTGAGGCCAG GACTGACGCC ACAGCCTGCA 1140
GCTCCTCCCC AAGCCCAGCC CCAGCCCTTG CCCTTCAATC CTGAGACCCT GAGATGCATG 1200
GGTGGGGCTT TCATCCGGTG AGGAGCGGAG GCCCAGGGAG GTGGGTTCCC CAGCTGCCAG 1260
TACCCACTGG TCAGGCTGGG CTGGACCAGG TCCTGAATCC CCGCCCTTCC ACCCATGGGC 1320
TCCCCAGGAA GGCTAAACTG AGGGAAGAAT TCCTGCTGGG AAAGCCCTGT TCTGGGACCA 1380
GGGTTTCGTC CCTCTATTAG AGGGGGTCAG GGGGACACCT GGGAGCGGAA CACCTGAGGG 1440
AGGAGCACCT GGCGGGGAGC CTTGGGGGAG GAGGCACCTG GGGGAGGAAG TCTGGAGGAG 1500
GGGTCTCCTG GTGGGGGGCC TGGAGGAGGG GTCTCCTGGG GGAGGGGCCT GGAGGAGGGG 1560
TCTCCTGGGG GAGGGGCCTG GAGGAGGGGT CTCCTGGGGG AGGGGCCTGG AGGAGGGGTC 1620
TCCTGGGGGG GGGCCTGGAG GAGGGGTCTC CTGGGGGAGG GGCCTGGAGG AGGGGTCTCC 1680
TGGGGGAGGG GCCCTTGGGG AGCCAACCCT AGTCAGTACG AGGTCCTGGG TGCAAAGTGG 1740
GTTGTGCGGC AGGGGGCTTG GGGCCTCAGC GGGGCTGCCC GGAGCTGGTC CTGGGCCTCT 1800
CTTGCTCTGG GTCTCCCCTG CTCTGGGTCC AGCCTCCCAA GCACCCCACC TGGCAAGACT 1860
TCCTCGCTCA GAACAGAGCC AACCCTGGCT GTCTTCCCAG GGTTTGTCGT GGAGAGGGCT 1920
CTGGCCCTTT AGCCTTCCAA GGAGCTTTCG GGGTTGGGGT ACGTTTGTGA CCCCAGTAGC 1980
CGCTGTGCTG GGGGCCCAGG GCAACTCCTC CGGGAGCAGG GAAGGCACTG CTGGCACCAC 2040
CAGCCCCGCA GGGTCACCAG CATCCCGTCT CCACCAGGGC TGCTGCTGTC CCTCCTCTGC 2100
TGAGGCCAGC TGTTACCGTG TTCGACATGG ACCAGGCCGT GTGGGAGGAC ACGGGGTGGC 2160
AGGTGCAGGG AGCACGGTCT GTTTTCTGTC ACTCTCTGGT CCCAGCCTGA GCCCCAATCC 2220
CTACCTCTGA GGGTCACACT TCCAACCCAC CCCAGACAGA GCTGGAAGCA GGGGCTGGCA 2280
TGGGCGCTGG GGTAGACGCA GGGGTTGTCG TGGCCTGGCG TGGAAGAGCT GGGCTGGACG 2340
CAGTGGGTGG CGTGGCCTGG GGTGCTGCTC TCCAGCCTTC TTTCTCTTCT TCCTCTTCCT 2400
CTTGTTCTTC ATCTTCCTCC TCTTGCTGCA GATCCTCCCC CAGGTGGCTC CATTTCTGCT 2460
GGTCCCATCT CCCGGAGGCC CTGCCCACAA CCCCCTGCCC GCCATCTAGG GGGACCCTGG 2520
CGTGGTCCAG GAGAGGGAGT CAAGGCCTGT GTGGGGCTCC TGGGGCTGGA GTCCTGGTCT 2580
GCCTTCTGGG GACAGAGACT AGGTCGCCCT GGGCTCCAGC TCTGTGGCCT GGCTGTGTGG 2640
GCTGGGCCAG GGCCTCTGCG TCACCTCCTT GCCTGGGCTT CTCACAGTGC AAGCCCCGCA 2700
GCCTAGGCCC TGCTGGGTGG TGGTGGGATG GCTGGGGAGG GGCAAGAGCA GGTGAGGAGT 2760
CCTCACTGGG GGTGCATACT TTGCATTACA GCTGGGGAGG CTGAGACCCG GGGGGCCACA 2820
GCTGGTTCCT GGACTCCAAA GCCCAGGACC 2850