EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS154-03127 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr10:112184860-112187500 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11195128chr10112186148hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr10:112187417-112187435TCTTTTTTCCTTCCTTCC-6.79
EWSR1-FLI1MA0149.1chr10:112187345-112187363CCTTCCTTTCTTTCTTTC-7.02
EWSR1-FLI1MA0149.1chr10:112187429-112187447CCTTCCTTTCTTTCTTTC-7.02
EWSR1-FLI1MA0149.1chr10:112187421-112187439TTTTCCTTCCTTCCTTTC-7.66
EWSR1-FLI1MA0149.1chr10:112187333-112187351TTCTCCTTCCTTCCTTCC-7.67
EWSR1-FLI1MA0149.1chr10:112187341-112187359CCTTCCTTCCTTTCTTTC-8.57
EWSR1-FLI1MA0149.1chr10:112187425-112187443CCTTCCTTCCTTTCTTTC-8.57
EWSR1-FLI1MA0149.1chr10:112187337-112187355CCTTCCTTCCTTCCTTTC-9.6
Foxa2MA0047.2chr10:112186112-112186124TGTTTACATAGT+6.22
HSF1MA0486.2chr10:112185565-112185578TTCTGGAATATTC+6.48
IRF1MA0050.2chr10:112187437-112187458TCTTTCTTTCTCTTTCTTTCT+6.76
NEUROD2MA0668.1chr10:112186088-112186098ACCATATGGC-6.02
Nfe2l2MA0150.2chr10:112185808-112185823CACTCTGACTCAGCA+6.15
RREB1MA0073.1chr10:112185951-112185971GTGAAGGGGTTGGTTTGGTG-6.17
Sox3MA0514.1chr10:112186793-112186803AAAACAAAGG-6.02
TEAD1MA0090.2chr10:112186900-112186910CACATTCCAT+6.02
ZNF263MA0528.1chr10:112187333-112187354TTCTCCTTCCTTCCTTCCTTT-6.07
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_34624chr10:112166474-112192739HeLa
SE_43727chr10:112179907-112185396MM1S
SE_45114chr10:112184850-112187468NHLF
SE_46227chr10:112184707-112187511Osteoblasts
SE_56435chr10:112185126-112187495u87
SE_65942chr10:112186095-112187812Pancreatic_islets
SE_67385chr10:112179907-112185396MM1S
SE_67956chr10:112185126-112187495u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr10112185759112186089
chr10112186754112186909
Number: 1             
IDChromosomeStartEnd
GH10I110424chr10112184569112187494
Enhancer Sequence
ATGAACACCC CCTCCCAAAT AAATATGAAA GGGGCTGGAA GGGGTCAGGT GGTCAACTCT 60
CTCCAAGGTG CAACCAGAGG TAGCTGAGAC TAACATGACA TAGGTCCCTG TTGGAGGACG 120
ATGTCCCCAG TAAACCCAAA TTAATTGAGT GACACCATAA AAAAACAGAA TAGGGAGGAG 180
TGGGGAAGAC CAGTCCCTTT CCTTGTGTCC AGGGATCCCA CCCATCTACA CCTCCATCCT 240
CCAGTGCCTG GCTAAGGCCC TCCTTAGTGC CCGGGCACAG ACTGTGCTCT TCGGAGATGG 300
CTCAAGTGGG CTGTGTGCTT AGGGAGATGG GGCACATGAC TGTTAACTAC TTTAAAAGTC 360
CTCAATGGGT TTTTTGTTGT TTCTGTTTTT GAGATGGAGT TTTGCTCTTG TTGCCCAGGC 420
TGGAGTGCAA TGGCGTGACC TCAGCAACCT GCAACGTCCG CCTCCCAGAT TCAAGGGATT 480
CTCCTACCTC AGCCTCCCAA GTAGCTGGGA TTACAGGTGT CTGCCACCAC ACCCAGCTAA 540
TTTTTTGTAT TTTTAGTAGA GATGGGGTTT CACCATGTTG GTCAGGCTGG TCTCGAACTT 600
CTGACCTCAG GTGATCCACC CTCCTCGGCC TCCCAAAGTG TTGAAATTAC AGGCGTGAGC 660
CACCGTGCCC GACCCTGAAT GTTTCTGAAG CATGCTGTTT CTTCATTCTG GAATATTCAC 720
TAAAAGAGCC CCTACGAATA ATTAACCCAG TAGTAATAAT AATGCCCACC ATTTGTCATT 780
CTTTCTATGT GCTCTGTACA TTACACGTGC ATCTCAGTTT ATCCCAATCA GTAGGCGGTT 840
CCATCCTTCA ATTTCATTTT ACAAATGAAG AAACCAAAGC TCACAGGGGA CATGTAACTT 900
GCCGAAGTTC ACATAGCCAC AGAGGGCAGA AGCTGAATTC AAACCACTCA CTCTGACTCA 960
GCATCCACCT CAGAGCAGCC ATTCAGTGGC CTCTTGTGAC ACATAAAGCA AGAAGATACC 1020
AGTGAGTTTT TGGACCATGT CTTCTTGGTA AAGTTACCAT TAGTCTGACC ACAGATGTTT 1080
CTCAAGAAGC AGTGAAGGGG TTGGTTTGGT GATGTCAGTG GCCGGGGTCA GATGAACCAA 1140
ACCATTGCTA GGCTGTGATG TCTGAGGCTG CCCACGAACT GGTTATTGCC CAGATTTAAA 1200
AGAAAGGTGG AAAAAATTAT CCTAGTCTAC CATATGGCTC AGCCAGCCAT AGTGTTTACA 1260
TAGTCAGAAA AGGTCAACAC AGAATAGCGA TATAATCAAA ATTACCCTCT ACGGTGTGGC 1320
TGTATTGGGA AGAGAGAGGC GGGGGTGGGT GTGAGGCAAC AGGAGCTAAA AGAACTCCTG 1380
GTCTCCCAGG GCAGGAAATC AAGAAAAAAC TCCTAAAACT ACACAGATCA AGAAGAAACT 1440
ATGTGAGATG TTATTTAGAG ACATGAAAGT GAACATTCCA AAGAATCCGT TTCAAGAGTC 1500
GAAAGTGGCC ACCCTGGAGA TGGGTCAGGG CTGCAGTTGT TCATGACTAA CTTTGTACAT 1560
TTCTGAGAAA TCTATGCTTA TGTGTAACTT CTCTTAAAAT AAAAAATTTA ATAAAATCCA 1620
AAGCAAAAAC AAACAGAGCA ATTCTGGCCC CATTTGGGGA GGGAGTGGGC TGTGATTACG 1680
AGAATGAGGG CCCAGCGGGT GGGGATTCCT CTGTCAGGCA TGCAACGGGA AGCTGGTGGG 1740
GTCTTGGCAA GGCTTTGGTG GAGAGACGTC ATTGGAATGG TGACCTCATT TGGAACCGGT 1800
GAGGGCAGGA GAAGGTAGAA GGGTTAAAAA GAAGAAGAAC CACCAAAGGA GAAGAAAAGG 1860
AAGCCTGGTC ATTCTACAGC CAAGGTCATA CTCCCAGGAG ACCTACGGCC TTTTGTCGGG 1920
GTTACACAAA TGTAAAACAA AGGTGTGGTC TCTCCACTAA ATGGGGAAGT TTCCACCAGG 1980
AGGCCAGTGT GTCATTGAGT AATGTGAATA GTGGAACCCA TCCCCAGCTA GTCAGGCCCA 2040
CACATTCCAT ACCAGGACCC ACGGGCCTCG GGGGTAGAGG CAGGAAGGTA GCATTTGTCT 2100
ATTGTGAGAA CAAGCAGCTT ATGTAGACAT CAAAGGTCTC AGGATAGCGT ATATTCTTCC 2160
AGATCTGTGA GGCCCAAACA CACACACATG GAGGAGGATC CCAGGGTCTC AGCCCCTCCC 2220
CAGATTCTCA AGACTCAGGC CTTGTCCCCT CTCCCATGGG GGTCCTATTG AAAGGAATCC 2280
AGAGACCCTG GGAGAATCTG AGTAGGAAGA GGGAACTGGA CTTACTGCCA TAGGCCCAGG 2340
CCTGGGTCAG GACTGTGTCT CTCTGGAAAA GCCACTCTCT TGGGAACTGA GAAAGCCCAG 2400
AGCTTGGGCC CAGAGCAGCC CAGGCCTTGA CTGGCCTGCC TGTTCCGTCC TCCTGTCTTC 2460
TCCAGGAAGC ATTTTCTCCT TCCTTCCTTC CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT 2520
TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTTTTCCTTC CTTCCTTTCT 2580
TTCTTTCTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT 2640