EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-04909 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr10:134220790-134223370 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs74383458chr10134221545hg19
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GabpaMA0062.2chr10:134221557-134221568CCGGAAGTGGA+6.32
PLAG1MA0163.1chr10:134223204-134223218GGGGCCAAATGGGG+6.75
RREB1MA0073.1chr10:134223129-134223149TCACCACCCACCCACCCACC+6.38
RREB1MA0073.1chr10:134223145-134223165CACCCACCCACCCACACCTC+6
RREB1MA0073.1chr10:134223133-134223153CACCCACCCACCCACCCACC+7.33
RREB1MA0073.1chr10:134223137-134223157CACCCACCCACCCACCCACC+7.33
RREB1MA0073.1chr10:134223141-134223161CACCCACCCACCCACCCACA+7.33
TFAP2AMA0003.3chr10:134222187-134222198TGCCTGAGGCA-6.02
ZNF263MA0528.1chr10:134223272-134223293TGAGAAGGAAGGGAAGAGGGG+6.29
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: 3             
ChromosomeStartEnd
chr10134221496134221692
chr10134221970134222202
chr10134222000134223200
Enhancer Sequence
CCCTCTGTGC TCTTCTTCCT GGCTCCATGG CCTAACCACC CCATGGATGC AGAGATTCCA 60
GGGCCAGGGG CTGTACGCAG AGGGCAGGGG CAGGGCTCCG CCTAGGCCTT GGTGACGTCT 120
GGTGACCTTG TCTTCCCTGG CCACCTGCCC AGAGGCCTTA GAGTTTCCCA GGTGACCGTC 180
CTCGGGCCTT TGTTGGGGGC GGGGACTGGA GCGCCTGGTG CCCCTCCACT GCTGCACCCT 240
GCGTATTGGG GTTCCGGCGG AAGCAGTGAT GAGAGACCAC TGTGGTTGAG CCAGGGTCCC 300
CAGGGTCCCC AGGCTGCCTG GCTGCCCAGG CTCTGGCCTG GCCTCACCCC CTCCCTCCAG 360
CCACCCGGCT GCATCTGCCT TGCTCTCCTG AGGCCAGGCA CAAACCTGGC TGCTCCCCCC 420
GCCCCAGGAA CCAGGCCCTT TTCTGATCAG TTCTGGGGCC TTGGGGCAGG CGTGGGGCAG 480
GTGCCTTGTT GGCGAGTGGG TGTGGGTGCC GTCTCTCAGC TTGAGTCTGG GGAGTGTCTC 540
AAGCCAGGGC ACCATCTTCT GAGGGGTAGG AGGAGGGTCA GAGGACTCCC GTCTGCTGTC 600
CTGGGGGGCC CTCCCCGAGT TCTGGACTCA GGCATTTGCG AGGCATGACA TCCCCCCACG 660
CAGGACGTCT CCAAGTGAGG CCTGAGGCCT TGGCTGGCAG GGAGTGCCCA GCCGGGAGGG 720
AGGACGGGAG GACACAGTCT TGCAGGCTCA GGGCCGGCTG TGTTTATCCG GAAGTGGAGG 780
AAGAATCTCA CCAGACGGGT TTGCCTGCCT CCACGGGGGG CAGTGCCTGC ACACGGGGCC 840
TGCGCCGGGA CCAGCCCCCT GCTCTGGGAG TGGGGGTGCC GGATCCTTTC AGCACCAAAG 900
CGCAGAGTGG TGTGTGCCTG GTTGGCTTTT TGGTCTTATT TCCTGAGGGC TAAAGACCAA 960
GTGCTCAGTG TGATCAGAGC TGGTGTCTCG TGGGGCCTGG GATCTCCCGC CCTCTGTGGG 1020
GTTGGTGGTC CTTGAGGGAC ACGTTTGCTT TGAAGTGTCA GCAGCGCACC TCTGGTCTGC 1080
TCTTTGTAGG GGAAATGCGG GGGTACCTGC CTTTCCTGGG AAGGGGGACC CGCCACCACC 1140
ATCGTGAAGG CGCCTCTCTG AGCAGAGGCT GAGTGAGGTG TGGGGCGCTG CTGGCCATGC 1200
CCGAGGGAGG GGCGGGAGGA GGAGGCTGGT GTGGGGGCTG GAGCTCGGGC AGGGAGGCCT 1260
TCCGGGGAAG GTCGTCCTCC CAGCTCCCGC CCACCGGCCA CCCTGGCCTG GCCCCAGCCG 1320
CTCCTGCAGC TGCCCGAGGA TGAGGACGGG GATGGCTGGG CGGTGTCAGA AGCTTCCTGA 1380
GGTTTGTGGG TGTCTGCTGC CTGAGGCACT TGTCAAGGAG CAGTCACCGC AGGCACCACG 1440
AGATCGGCTC CGTTGCAGGG ACACTGAGCC CAGCATCTAC CCATGAGAGA CCCCTCACTC 1500
TCTCTCAGCT TGCTGCGGGG CTGGAGGCCC TGCTCAGGGG TAGGCGGATG CCCCACAGAC 1560
CACAGGGTGC CAGGGCATTG GGCCTGTGGC CGGCAGTGCC AAGAGGCAGC CTGGCTGGCA 1620
CAAGGGACGG GCACATCGGC CTCAGCAGGG GCCGCGCCAG GACGCATGGC TGTGACACAC 1680
TTGGGCACCC CTCCGTGTGA GGTCCTGATG GAGGTGCGCC GAGGCTGGGC TGGCCTCCTG 1740
TGCAGGAATA GAGGCCGTTG GGCCTTGTCC CAGCCGGTCA CCTGCTGTTG CGGTCTCAGG 1800
GAGCCAACAC CTCTGAGCCT GTTTGTTCAC CGCTCCCAGG GTAACAACAG GTCCCGCCTC 1860
TGAGTGAGCC GCACTCCACC CCGGTGGTCA CGGCCGGCTC CAGGGCCTGT GAATGGCCTG 1920
TGGCCGCTGC CCTTGGAGGT GACCACTGTG CCCTCTCAGG CTGGCAGGAG AGGCCGTTCC 1980
CTGGGACTTC TCCTACACCC ACAGGGACCC CATGGGATTA GAGCTGAGGT CCGGGGCGGG 2040
GGCAGGTGGT GGAGACCAGG CTCTGGGGTT ACTGTGCCTG GGAGCAGCCT CCTGCTTCAG 2100
GTGCAGGCAC CGGACATGCA GGGTCAGGGG CCCAGCAGGA GCTGCCTGGC CAGGCTTGTC 2160
CTGCAGCTGG GAATGGGGAC CCAGAGAAGG CAATGCCACC CACACCCCCA CCACCGCCTG 2220
GGCCCACCGA GCCTGAGAGG GGAAGGCAGC TCCTCCCCAG GGTGAGCCCC AGGGCCTCGG 2280
GCTGGGGTCC TGCCCCTGTC CAGGCTCAAG GTCCTCTCTC TGCTCCCCTG GTCTCTCCCT 2340
CACCACCCAC CCACCCACCC ACCCACCCAC ACCTCTACTG AGGGCCAAGC ACTCCACTGG 2400
GCCCAGGCTA GAAGGGGGCC AAATGGGGAG GGCTGTGAAT CACCAGTTCC CAAATTAGTG 2460
CATAATCACA CACAGGAACT GCTGAGAAGG AAGGGAAGAG GGGCTTGAAG CAGAGCATCC 2520
AGCGAGAAAC CTGGCCTGGA CTGGGATCCG GGAAGGCTTC CTGGAGGAGG TGGCAGGAGC 2580