EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS179-05637 
Organism
Homo sapiens 
Tissue/cell
SkMC 
Coordinate
chr10:112184600-112187460 
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
ACCATGTTTC CCAAGCTGGT CTAGAACTCT TGGGCTCAAG TGATCCACCT GCCTCGGCCT 60
CCCAAAGTGC TGTGATGACA GGTGTGAGCC ATGGCGCACG GTCCCCCATG CACATTTAAA 120
GCATGGAAAA TAAAATCCTG GAAGGACACA TGGCAAACTG TTAACAGCAT TTACCTCTAA 180
GGTAGAAAAA AGATCTTAAA TTTTTTCTTT TATACTTCTG CACTGTTTGA ATCTCTTAAA 240
ATTAGCACAT ACTATATATG ATGAACACCC CCTCCCAAAT AAATATGAAA GGGGCTGGAA 300
GGGGTCAGGT GGTCAACTCT CTCCAAGGTG CAACCAGAGG TAGCTGAGAC TAACATGACA 360
TAGGTCCCTG TTGGAGGACG ATGTCCCCAG TAAACCCAAA TTAATTGAGT GACACCATAA 420
AAAAACAGAA TAGGGAGGAG TGGGGAAGAC CAGTCCCTTT CCTTGTGTCC AGGGATCCCA 480
CCCATCTACA CCTCCATCCT CCAGTGCCTG GCTAAGGCCC TCCTTAGTGC CCGGGCACAG 540
ACTGTGCTCT TCGGAGATGG CTCAAGTGGG CTGTGTGCTT AGGGAGATGG GGCACATGAC 600
TGTTAACTAC TTTAAAAGTC CTCAATGGGT TTTTTGTTGT TTCTGTTTTT GAGATGGAGT 660
TTTGCTCTTG TTGCCCAGGC TGGAGTGCAA TGGCGTGACC TCAGCAACCT GCAACGTCCG 720
CCTCCCAGAT TCAAGGGATT CTCCTACCTC AGCCTCCCAA GTAGCTGGGA TTACAGGTGT 780
CTGCCACCAC ACCCAGCTAA TTTTTTGTAT TTTTAGTAGA GATGGGGTTT CACCATGTTG 840
GTCAGGCTGG TCTCGAACTT CTGACCTCAG GTGATCCACC CTCCTCGGCC TCCCAAAGTG 900
TTGAAATTAC AGGCGTGAGC CACCGTGCCC GACCCTGAAT GTTTCTGAAG CATGCTGTTT 960
CTTCATTCTG GAATATTCAC TAAAAGAGCC CCTACGAATA ATTAACCCAG TAGTAATAAT 1020
AATGCCCACC ATTTGTCATT CTTTCTATGT GCTCTGTACA TTACACGTGC ATCTCAGTTT 1080
ATCCCAATCA GTAGGCGGTT CCATCCTTCA ATTTCATTTT ACAAATGAAG AAACCAAAGC 1140
TCACAGGGGA CATGTAACTT GCCGAAGTTC ACATAGCCAC AGAGGGCAGA AGCTGAATTC 1200
AAACCACTCA CTCTGACTCA GCATCCACCT CAGAGCAGCC ATTCAGTGGC CTCTTGTGAC 1260
ACATAAAGCA AGAAGATACC AGTGAGTTTT TGGACCATGT CTTCTTGGTA AAGTTACCAT 1320
TAGTCTGACC ACAGATGTTT CTCAAGAAGC AGTGAAGGGG TTGGTTTGGT GATGTCAGTG 1380
GCCGGGGTCA GATGAACCAA ACCATTGCTA GGCTGTGATG TCTGAGGCTG CCCACGAACT 1440
GGTTATTGCC CAGATTTAAA AGAAAGGTGG AAAAAATTAT CCTAGTCTAC CATATGGCTC 1500
AGCCAGCCAT AGTGTTTACA TAGTCAGAAA AGGTCAACAC AGAATAGCGA TATAATCAAA 1560
ATTACCCTCT ACGGTGTGGC TGTATTGGGA AGAGAGAGGC GGGGGTGGGT GTGAGGCAAC 1620
AGGAGCTAAA AGAACTCCTG GTCTCCCAGG GCAGGAAATC AAGAAAAAAC TCCTAAAACT 1680
ACACAGATCA AGAAGAAACT ATGTGAGATG TTATTTAGAG ACATGAAAGT GAACATTCCA 1740
AAGAATCCGT TTCAAGAGTC GAAAGTGGCC ACCCTGGAGA TGGGTCAGGG CTGCAGTTGT 1800
TCATGACTAA CTTTGTACAT TTCTGAGAAA TCTATGCTTA TGTGTAACTT CTCTTAAAAT 1860
AAAAAATTTA ATAAAATCCA AAGCAAAAAC AAACAGAGCA ATTCTGGCCC CATTTGGGGA 1920
GGGAGTGGGC TGTGATTACG AGAATGAGGG CCCAGCGGGT GGGGATTCCT CTGTCAGGCA 1980
TGCAACGGGA AGCTGGTGGG GTCTTGGCAA GGCTTTGGTG GAGAGACGTC ATTGGAATGG 2040
TGACCTCATT TGGAACCGGT GAGGGCAGGA GAAGGTAGAA GGGTTAAAAA GAAGAAGAAC 2100
CACCAAAGGA GAAGAAAAGG AAGCCTGGTC ATTCTACAGC CAAGGTCATA CTCCCAGGAG 2160
ACCTACGGCC TTTTGTCGGG GTTACACAAA TGTAAAACAA AGGTGTGGTC TCTCCACTAA 2220
ATGGGGAAGT TTCCACCAGG AGGCCAGTGT GTCATTGAGT AATGTGAATA GTGGAACCCA 2280
TCCCCAGCTA GTCAGGCCCA CACATTCCAT ACCAGGACCC ACGGGCCTCG GGGGTAGAGG 2340
CAGGAAGGTA GCATTTGTCT ATTGTGAGAA CAAGCAGCTT ATGTAGACAT CAAAGGTCTC 2400
AGGATAGCGT ATATTCTTCC AGATCTGTGA GGCCCAAACA CACACACATG GAGGAGGATC 2460
CCAGGGTCTC AGCCCCTCCC CAGATTCTCA AGACTCAGGC CTTGTCCCCT CTCCCATGGG 2520
GGTCCTATTG AAAGGAATCC AGAGACCCTG GGAGAATCTG AGTAGGAAGA GGGAACTGGA 2580
CTTACTGCCA TAGGCCCAGG CCTGGGTCAG GACTGTGTCT CTCTGGAAAA GCCACTCTCT 2640
TGGGAACTGA GAAAGCCCAG AGCTTGGGCC CAGAGCAGCC CAGGCCTTGA CTGGCCTGCC 2700
TGTTCCGTCC TCCTGTCTTC TCCAGGAAGC ATTTTCTCCT TCCTTCCTTC CTTTCTTTCT 2760
TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT 2820
TTTTTCCTTC CTTCCTTTCT TTCTTTCTCT TTCTTTCTTT 2860