EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-04892 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr10:112593160-112595620 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ALX3MA0634.1chr10:112595270-112595280TTTAATTAGA-6.02
INSM1MA0155.1chr10:112593453-112593465CGCCCCCAGGCA-6.14
KLF16MA0741.1chr10:112593449-112593460GCCACGCCCCC+6.62
Nr5a2MA0505.1chr10:112593337-112593352TAGTTCAAGGTCACC+6.87
SP1MA0079.4chr10:112593446-112593461TGGGCCACGCCCCCA+6
SP3MA0746.2chr10:112593448-112593461GGCCACGCCCCCA+6.57
SP8MA0747.1chr10:112593449-112593461GCCACGCCCCCA+6.11
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01940chr10:112593158-112595091Aorta
SE_01940chr10:112595144-112596465Aorta
SE_23151chr10:112593837-112595059Colon_Crypt_1
SE_24035chr10:112593896-112594299Colon_Crypt_2
SE_24035chr10:112594402-112594960Colon_Crypt_2
SE_25029chr10:112593227-112595085Colon_Crypt_3
SE_25029chr10:112595324-112596350Colon_Crypt_3
SE_26657chr10:112593027-112598717Esophagus
SE_27704chr10:112593156-112595214Fetal_Intestine
SE_27704chr10:112595240-112607543Fetal_Intestine
SE_28632chr10:112593028-112607614Fetal_Intestine_Large
SE_30685chr10:112593035-112595992Fetal_Muscle
SE_31444chr10:112592993-112598574Gastric
SE_33439chr10:112592285-112599612H2171
SE_40590chr10:112593153-112595210Left_Ventricle
SE_40590chr10:112595240-112598049Left_Ventricle
SE_42131chr10:112593162-112595078Lung
SE_47093chr10:112593628-112594854Ovary
SE_47093chr10:112595360-112596395Ovary
SE_47589chr10:112593247-112595033Pancreas
SE_47589chr10:112595335-112595999Pancreas
SE_48568chr10:112593205-112595184Right_Atrium
SE_48568chr10:112595300-112596511Right_Atrium
SE_52404chr10:112593498-112595083Small_Intestine
SE_58452chr10:112593100-112642895Ly1
SE_59745chr10:112593531-112634215Ly4
SE_60982chr10:112552689-112654127HBL1
SE_62307chr10:112592977-112644561Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10112593200112593706
Number: 1             
IDChromosomeStartEnd
GH10I110832chr10112592568112607580
Enhancer Sequence
AAAAGAAATG CAGCTTCCTG GCTCTCACCC TACTCTTGTT TTCTCATTTT CTGTAGGGCT 60
GGGCCTGAGA GTCTGTATTG TAAACCATCC TTATATCAGG CTCTGATAGT CGATGTGAGA 120
ACCTTTTCTC TCATCCAGCA TTTGCAGTAG TATTGTGCAG CCCTTCAGGG GGCCACATAG 180
TTCAAGGTCA CCTCGGAAGT TAGGAAGAGT TCAGACTTGC CAGGGCCTCT AATTCTAATT 240
CATGTATGTT TCCCAGGGCA GTGGACTGCA CTGTGTTCTG AGCCTCTGGG CCACGCCCCC 300
AGGCAGACTC CCCTCCCCGC AGCAGGCCAG AGCCATTCTT GTAGTTCTCA AGTGCATTGG 360
GGTAGACATT GGTTAAGCCC CTCGTGCCAG CCAACTGCAG TGTAGCTTTA CCTGGTGCAC 420
CTGCTGGGGA GCTGGGAGTT TCCACCACAG GCTTCCCAGA TAGGATTTCT GTCAGCGGCT 480
TTGACAGAAT GCCTCTGTCC ACACAGCCTC CCCCACCCCA AGCAGCAGGT AATGGCTGAC 540
ACTTAAATCA GGCAACTTTT AAACTTAACA CCACTGAGAG GCCTTGAGTT GGGGACCAGA 600
GGTTGCTCCT AAAGGCAGGG AGCAGGTTGA AGGAGCCTCC GCTCTCTCTG AGCAGCCTGT 660
GCTGTGCCCC ACGGCTGGTC ACGGCTCTGC AAGAACCCAC CCAGAGTGAT TCAGAACAAC 720
AGGTGGAGTC AGCGCTCGAT AGGAAAACTA GATACCTGCT TGGCTCCAGG CCCTGGAGCG 780
GAATGTGTCC ACGTACTGGG CGCTCATTCG CTTGCCTTCC TCAGCACACG GTTTACCCTC 840
CCTGAGCCAA GGCAGAGGAG AACCCAGGCC CTCCATCAGC AGCTTTGCCT GCTGCCATCC 900
ACCGTTTGCT CTTCTCCTAG TCAGGCTGCA CCCGTTTCTG GAAGCCAACT GCAGTCTCTT 960
CTATGGAGAC AGCAGGCAGA CCTGGTCATC TCACACACAC CCTCTCATCT GACCCACACA 1020
CCACCCCAGA AGGGAGGGTG AGGACAACAG TGTTCCTCCC ATTTAACAGA TTAGGCCTCT 1080
GAGGCTGGGA GAAGAGGAGT GGCTTTCTCC AACTCATATG GCTGGTGCTG CTAATAAGAA 1140
AAGCCAACAT TACTGAGTGT TTATTCTGTG TCAAACGCTG TACTGAATGC TTTTTGTTGC 1200
CTCTCTTCGA CTTCACAGCA ACCTTATGTT GTTGTTACTG TTATTCCCCT CCCTTCACAG 1260
ATGTCAGAGA TATTTGATAA CTCGCCTGCT GAGGGATAGG ATTGAACCCA GGTCATATGA 1320
CTTCAAAGTG CACACACTTA ACCACCGTAC TGGTCTGCAC CCTTCTGTCT CCTAATCCAG 1380
TGCTCTTTGC CTTTTCCTTG CTGCCCTGTC AGAGAACCCC AGCTGGGGCC TCAAACCTGT 1440
CCCAGTCTGC CTCACTGTGT TGACTCCAGA TAGCCCAAGA GCAACCCAAC CTGCCTCATG 1500
GTGTTGGGCC GAGGCCAGTC ATAGCAGTGA GTGTTCTGGG GTCATGCAGA GGCAGCCCTC 1560
AACGATAGAA TAGACAGGCC CATTTTTAAA TCCATCAAAA GACCTCCAAG GCTCCCCACC 1620
CACTAGCCTG CCCTGACAGG AAACAGGTTG TTAAGAGTCT CAAATGTCAG GCCGTGGTGC 1680
TGTTTTGCAC AATTGCCATA GGCCAGCGCT CATTTACCCT GCCTTCCAGC TTCCCTCCCT 1740
CTGCCTTTTA AGCATAGATA TGTTGCCTAG AGCTTGGGCT GTTTCTGGAA AACAGAGTTG 1800
TTTTGGGAGT TAAATGAGCT TATTTAAGTC AAGCAGTTAG AACAGCACTT GACACTAGAT 1860
AAGGGCTTTG GAAGTGTTTG CTATTATAGC TGTACTTTCT ACTCTTTCTT TTCTTTTCTT 1920
TTTTTCTTTT TTTTTTCTTT TTTTTTTTTT TAGATGGAGT TTCACTCTTG TTGCCCAGGC 1980
TGGATTGCAA CGGTGCGATC TCGGTTCACA GCAACCTCCG CCTCCCGGGT TCAAGTGATT 2040
CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA TTACAGGCAT GTGCCACCAC ACCCAGCTAA 2100
TTTTTTGTAT TTTAATTAGA GACGGGGTTT CTCCATGTTG GTCAGGCTGG TCTCAACTCC 2160
CGACCTCAGG TGATCCACCC ACCTCGGCCT CCCAAGTGCT GGGATTACAG GTGTGAGACA 2220
CCACGCTCGG CCTGTACTTT CTACATTTTC TACAGGAGAC ATGTATTACT TGCAAGCTAA 2280
CATAATGAGG TACTTAGCAT AAGTTCTGTA GCCCCAGTGG GGATCTCTGA ACCAGGAAAA 2340
GGGTAACCCC CACAGCTGGG CACAGATGCC AGGAGAGGGA TGATTGAGGC ATGTCCGCTC 2400
CTCTCCTCTC CATCTAGGTC CCTACTAACA TGCCCCTTCC TCCACTTCCC CTCTTCTTTC 2460