EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS120-01004 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr10:134220560-134223160 
Target genes
Number: 3             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs74383458chr10134221545hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GabpaMA0062.2chr10:134221557-134221568CCGGAAGTGGA+6.32
RREB1MA0073.1chr10:134223129-134223149TCACCACCCACCCACCCACC+6.38
RREB1MA0073.1chr10:134223133-134223153CACCCACCCACCCACCCACC+7.33
RREB1MA0073.1chr10:134223137-134223157CACCCACCCACCCACCCACC+7.33
TFAP2AMA0003.3chr10:134222187-134222198TGCCTGAGGCA-6.02
ZNF263MA0528.1chr10:134221992-134222013GAGGGAGGGGCGGGAGGAGGA+7.74
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00873chr10:134218800-134226717Adrenal_Gland
SE_02964chr10:134220377-134223463Bladder
SE_04410chr10:134220363-134222950Brain_Anterior_Caudate
SE_09804chr10:134220280-134222532CD14
SE_10426chr10:134221360-134222162CD19_Primary
SE_11568chr10:134220135-134222912CD20
SE_23061chr10:134219282-134226762Colon_Crypt_1
SE_23725chr10:134219686-134223556Colon_Crypt_2
SE_24681chr10:134207224-134228585Colon_Crypt_3
SE_26753chr10:134219639-134228593Esophagus
SE_28153chr10:134220141-134223109Fetal_Intestine
SE_29112chr10:134220142-134223149Fetal_Intestine_Large
SE_31406chr10:134219015-134228553Gastric
SE_33290chr10:134220340-134223251H1
SE_34405chr10:134219619-134223123HCT-116
SE_41567chr10:134219041-134226713LNCaP
SE_42252chr10:134219499-134237674Lung
SE_47467chr10:134219234-134226760Pancreas
SE_50143chr10:134219172-134226712Sigmoid_Colon
SE_53287chr10:134219205-134237202Spleen
SE_56893chr10:134220205-134223564VACO_400
SE_57427chr10:134220150-134223273VACO_503
SE_57946chr10:134219984-134223521VACO_9m
SE_61428chr10:134196155-134334764Toledo
SE_65264chr10:134210665-134236634Pancreatic_islets
SE_68705chr10:134218519-134226778H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10134221496134221692
chr10134221970134222202
Enhancer Sequence
TGGAGGTGTG GGGGTGTCAC CTTGTGGGGC TGGGGGCACC ACCCATGCCC CTGTAATCAC 60
CACGTGGGGC ATCCGGAGCC TGCCGAGGGG CTGTTTTCTG CCCTGAGCTC CTGAAGGCCA 120
CTCTCCCAGC TCCAGAGGCC TTCTCAGCAC CTCCTAGATG CCCCTCTTGT CTTCCCAGCA 180
GGAGAAGGCA GGCCAGGGAG CAGTCCTTTC TGGGTGGGGG CAGCTGGTGG CCCTCTGTGC 240
TCTTCTTCCT GGCTCCATGG CCTAACCACC CCATGGATGC AGAGATTCCA GGGCCAGGGG 300
CTGTACGCAG AGGGCAGGGG CAGGGCTCCG CCTAGGCCTT GGTGACGTCT GGTGACCTTG 360
TCTTCCCTGG CCACCTGCCC AGAGGCCTTA GAGTTTCCCA GGTGACCGTC CTCGGGCCTT 420
TGTTGGGGGC GGGGACTGGA GCGCCTGGTG CCCCTCCACT GCTGCACCCT GCGTATTGGG 480
GTTCCGGCGG AAGCAGTGAT GAGAGACCAC TGTGGTTGAG CCAGGGTCCC CAGGGTCCCC 540
AGGCTGCCTG GCTGCCCAGG CTCTGGCCTG GCCTCACCCC CTCCCTCCAG CCACCCGGCT 600
GCATCTGCCT TGCTCTCCTG AGGCCAGGCA CAAACCTGGC TGCTCCCCCC GCCCCAGGAA 660
CCAGGCCCTT TTCTGATCAG TTCTGGGGCC TTGGGGCAGG CGTGGGGCAG GTGCCTTGTT 720
GGCGAGTGGG TGTGGGTGCC GTCTCTCAGC TTGAGTCTGG GGAGTGTCTC AAGCCAGGGC 780
ACCATCTTCT GAGGGGTAGG AGGAGGGTCA GAGGACTCCC GTCTGCTGTC CTGGGGGGCC 840
CTCCCCGAGT TCTGGACTCA GGCATTTGCG AGGCATGACA TCCCCCCACG CAGGACGTCT 900
CCAAGTGAGG CCTGAGGCCT TGGCTGGCAG GGAGTGCCCA GCCGGGAGGG AGGACGGGAG 960
GACACAGTCT TGCAGGCTCA GGGCCGGCTG TGTTTATCCG GAAGTGGAGG AAGAATCTCA 1020
CCAGACGGGT TTGCCTGCCT CCACGGGGGG CAGTGCCTGC ACACGGGGCC TGCGCCGGGA 1080
CCAGCCCCCT GCTCTGGGAG TGGGGGTGCC GGATCCTTTC AGCACCAAAG CGCAGAGTGG 1140
TGTGTGCCTG GTTGGCTTTT TGGTCTTATT TCCTGAGGGC TAAAGACCAA GTGCTCAGTG 1200
TGATCAGAGC TGGTGTCTCG TGGGGCCTGG GATCTCCCGC CCTCTGTGGG GTTGGTGGTC 1260
CTTGAGGGAC ACGTTTGCTT TGAAGTGTCA GCAGCGCACC TCTGGTCTGC TCTTTGTAGG 1320
GGAAATGCGG GGGTACCTGC CTTTCCTGGG AAGGGGGACC CGCCACCACC ATCGTGAAGG 1380
CGCCTCTCTG AGCAGAGGCT GAGTGAGGTG TGGGGCGCTG CTGGCCATGC CCGAGGGAGG 1440
GGCGGGAGGA GGAGGCTGGT GTGGGGGCTG GAGCTCGGGC AGGGAGGCCT TCCGGGGAAG 1500
GTCGTCCTCC CAGCTCCCGC CCACCGGCCA CCCTGGCCTG GCCCCAGCCG CTCCTGCAGC 1560
TGCCCGAGGA TGAGGACGGG GATGGCTGGG CGGTGTCAGA AGCTTCCTGA GGTTTGTGGG 1620
TGTCTGCTGC CTGAGGCACT TGTCAAGGAG CAGTCACCGC AGGCACCACG AGATCGGCTC 1680
CGTTGCAGGG ACACTGAGCC CAGCATCTAC CCATGAGAGA CCCCTCACTC TCTCTCAGCT 1740
TGCTGCGGGG CTGGAGGCCC TGCTCAGGGG TAGGCGGATG CCCCACAGAC CACAGGGTGC 1800
CAGGGCATTG GGCCTGTGGC CGGCAGTGCC AAGAGGCAGC CTGGCTGGCA CAAGGGACGG 1860
GCACATCGGC CTCAGCAGGG GCCGCGCCAG GACGCATGGC TGTGACACAC TTGGGCACCC 1920
CTCCGTGTGA GGTCCTGATG GAGGTGCGCC GAGGCTGGGC TGGCCTCCTG TGCAGGAATA 1980
GAGGCCGTTG GGCCTTGTCC CAGCCGGTCA CCTGCTGTTG CGGTCTCAGG GAGCCAACAC 2040
CTCTGAGCCT GTTTGTTCAC CGCTCCCAGG GTAACAACAG GTCCCGCCTC TGAGTGAGCC 2100
GCACTCCACC CCGGTGGTCA CGGCCGGCTC CAGGGCCTGT GAATGGCCTG TGGCCGCTGC 2160
CCTTGGAGGT GACCACTGTG CCCTCTCAGG CTGGCAGGAG AGGCCGTTCC CTGGGACTTC 2220
TCCTACACCC ACAGGGACCC CATGGGATTA GAGCTGAGGT CCGGGGCGGG GGCAGGTGGT 2280
GGAGACCAGG CTCTGGGGTT ACTGTGCCTG GGAGCAGCCT CCTGCTTCAG GTGCAGGCAC 2340
CGGACATGCA GGGTCAGGGG CCCAGCAGGA GCTGCCTGGC CAGGCTTGTC CTGCAGCTGG 2400
GAATGGGGAC CCAGAGAAGG CAATGCCACC CACACCCCCA CCACCGCCTG GGCCCACCGA 2460
GCCTGAGAGG GGAAGGCAGC TCCTCCCCAG GGTGAGCCCC AGGGCCTCGG GCTGGGGTCC 2520
TGCCCCTGTC CAGGCTCAAG GTCCTCTCTC TGCTCCCCTG GTCTCTCCCT CACCACCCAC 2580
CCACCCACCC ACCCACCCAC 2600