EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-03867 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr10:112592510-112595620 
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: 25             
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_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_47589chr10:112593247-112595033Pancreas
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: 2             
ChromosomeStartEnd
chr10112593102112595074
chr10112593200112593706
Number: 1             
IDChromosomeStartEnd
GH10I110832chr10112592568112607580
Enhancer Sequence
TGCAGAGAAG TATCATAGGC TATGCCCAAA CTCAAGTCAC TTAAGCCTCT GATTTCCCTC 60
CGGAGAGCAG CTTCTCTGTG ACTGAGGCAG CCACAGCACC TGTGGCCCAG GGCTAGGCCT 120
CTCCTCGGGC AAGGCAAGAA AGGCCTGACT TGGCCAGAGC AGGAGGGTCA GACTGGGTCC 180
CACAAAGCCA GCTGAGGGAA GTCATCTAGC TTGAAGACAT AATCAATCCC TTTTCCCAAC 240
AAGATGAAAC CTACAGAATG GTAAGGATGG AAGGGGTCTT GGAAATCATC TGGTCCTGGT 300
TTTCCCAAAC CTTCTTCTTT GTACCAGCTG GCATCTTTTT GAAATGCAGC TTCCTGGGCC 360
CGGCACAGTG GCTCACACCT GTAATCCCAG CACTTTGGGA GACCGAGGCG GGTGGATCAC 420
GAGGTCAGGA ATTCGAGACC AGCCTGACCA ACAGTGTGAA ATCCCGTCTC TACTAAAAAT 480
ACAAAAACTA GCCAGGCGTG GTGGCGCGCA CCTATAATCC AAGCTACTCA GGAGGCTGAG 540
GTAGGAGAAT CGCTTGAACC TGGGAGGTGG AGCTTGCAGT GAGCCGAGAT CACATCATTG 600
CTCTCCAGCC TGGGTGACGG AGCGAAACTC TGTCTCAGAA AAAAAAAAAA AAAAGAAATG 660
CAGCTTCCTG GCTCTCACCC TACTCTTGTT TTCTCATTTT CTGTAGGGCT GGGCCTGAGA 720
GTCTGTATTG TAAACCATCC TTATATCAGG CTCTGATAGT CGATGTGAGA ACCTTTTCTC 780
TCATCCAGCA TTTGCAGTAG TATTGTGCAG CCCTTCAGGG GGCCACATAG TTCAAGGTCA 840
CCTCGGAAGT TAGGAAGAGT TCAGACTTGC CAGGGCCTCT AATTCTAATT CATGTATGTT 900
TCCCAGGGCA GTGGACTGCA CTGTGTTCTG AGCCTCTGGG CCACGCCCCC AGGCAGACTC 960
CCCTCCCCGC AGCAGGCCAG AGCCATTCTT GTAGTTCTCA AGTGCATTGG GGTAGACATT 1020
GGTTAAGCCC CTCGTGCCAG CCAACTGCAG TGTAGCTTTA CCTGGTGCAC CTGCTGGGGA 1080
GCTGGGAGTT TCCACCACAG GCTTCCCAGA TAGGATTTCT GTCAGCGGCT TTGACAGAAT 1140
GCCTCTGTCC ACACAGCCTC CCCCACCCCA AGCAGCAGGT AATGGCTGAC ACTTAAATCA 1200
GGCAACTTTT AAACTTAACA CCACTGAGAG GCCTTGAGTT GGGGACCAGA GGTTGCTCCT 1260
AAAGGCAGGG AGCAGGTTGA AGGAGCCTCC GCTCTCTCTG AGCAGCCTGT GCTGTGCCCC 1320
ACGGCTGGTC ACGGCTCTGC AAGAACCCAC CCAGAGTGAT TCAGAACAAC AGGTGGAGTC 1380
AGCGCTCGAT AGGAAAACTA GATACCTGCT TGGCTCCAGG CCCTGGAGCG GAATGTGTCC 1440
ACGTACTGGG CGCTCATTCG CTTGCCTTCC TCAGCACACG GTTTACCCTC CCTGAGCCAA 1500
GGCAGAGGAG AACCCAGGCC CTCCATCAGC AGCTTTGCCT GCTGCCATCC ACCGTTTGCT 1560
CTTCTCCTAG TCAGGCTGCA CCCGTTTCTG GAAGCCAACT GCAGTCTCTT CTATGGAGAC 1620
AGCAGGCAGA CCTGGTCATC TCACACACAC CCTCTCATCT GACCCACACA CCACCCCAGA 1680
AGGGAGGGTG AGGACAACAG TGTTCCTCCC ATTTAACAGA TTAGGCCTCT GAGGCTGGGA 1740
GAAGAGGAGT GGCTTTCTCC AACTCATATG GCTGGTGCTG CTAATAAGAA AAGCCAACAT 1800
TACTGAGTGT TTATTCTGTG TCAAACGCTG TACTGAATGC TTTTTGTTGC CTCTCTTCGA 1860
CTTCACAGCA ACCTTATGTT GTTGTTACTG TTATTCCCCT CCCTTCACAG ATGTCAGAGA 1920
TATTTGATAA CTCGCCTGCT GAGGGATAGG ATTGAACCCA GGTCATATGA CTTCAAAGTG 1980
CACACACTTA ACCACCGTAC TGGTCTGCAC CCTTCTGTCT CCTAATCCAG TGCTCTTTGC 2040
CTTTTCCTTG CTGCCCTGTC AGAGAACCCC AGCTGGGGCC TCAAACCTGT CCCAGTCTGC 2100
CTCACTGTGT TGACTCCAGA TAGCCCAAGA GCAACCCAAC CTGCCTCATG GTGTTGGGCC 2160
GAGGCCAGTC ATAGCAGTGA GTGTTCTGGG GTCATGCAGA GGCAGCCCTC AACGATAGAA 2220
TAGACAGGCC CATTTTTAAA TCCATCAAAA GACCTCCAAG GCTCCCCACC CACTAGCCTG 2280
CCCTGACAGG AAACAGGTTG TTAAGAGTCT CAAATGTCAG GCCGTGGTGC TGTTTTGCAC 2340
AATTGCCATA GGCCAGCGCT CATTTACCCT GCCTTCCAGC TTCCCTCCCT CTGCCTTTTA 2400
AGCATAGATA TGTTGCCTAG AGCTTGGGCT GTTTCTGGAA AACAGAGTTG TTTTGGGAGT 2460
TAAATGAGCT TATTTAAGTC AAGCAGTTAG AACAGCACTT GACACTAGAT AAGGGCTTTG 2520
GAAGTGTTTG CTATTATAGC TGTACTTTCT ACTCTTTCTT TTCTTTTCTT TTTTTCTTTT 2580
TTTTTTCTTT TTTTTTTTTT TAGATGGAGT TTCACTCTTG TTGCCCAGGC TGGATTGCAA 2640
CGGTGCGATC TCGGTTCACA GCAACCTCCG CCTCCCGGGT TCAAGTGATT CTCCTGCCTC 2700
AGCCTCCCGA GTAGCTGGGA TTACAGGCAT GTGCCACCAC ACCCAGCTAA TTTTTTGTAT 2760
TTTAATTAGA GACGGGGTTT CTCCATGTTG GTCAGGCTGG TCTCAACTCC CGACCTCAGG 2820
TGATCCACCC ACCTCGGCCT CCCAAGTGCT GGGATTACAG GTGTGAGACA CCACGCTCGG 2880
CCTGTACTTT CTACATTTTC TACAGGAGAC ATGTATTACT TGCAAGCTAA CATAATGAGG 2940
TACTTAGCAT AAGTTCTGTA GCCCCAGTGG GGATCTCTGA ACCAGGAAAA GGGTAACCCC 3000
CACAGCTGGG CACAGATGCC AGGAGAGGGA TGATTGAGGC ATGTCCGCTC CTCTCCTCTC 3060
CATCTAGGTC CCTACTAACA TGCCCCTTCC TCCACTTCCC CTCTTCTTTC 3110