EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS078-02841 
Organism
Homo sapiens 
Tissue/cell
H2171 
Coordinate
chr10:112593070-112595620 
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: 2             
ChromosomeStartEnd
chr10112593102112595074
chr10112593200112593706
Number: 1             
IDChromosomeStartEnd
GH10I110832chr10112592568112607580
Enhancer Sequence
TGGGAGGTGG AGCTTGCAGT GAGCCGAGAT CACATCATTG CTCTCCAGCC TGGGTGACGG 60
AGCGAAACTC TGTCTCAGAA AAAAAAAAAA AAAAGAAATG CAGCTTCCTG GCTCTCACCC 120
TACTCTTGTT TTCTCATTTT CTGTAGGGCT GGGCCTGAGA GTCTGTATTG TAAACCATCC 180
TTATATCAGG CTCTGATAGT CGATGTGAGA ACCTTTTCTC TCATCCAGCA TTTGCAGTAG 240
TATTGTGCAG CCCTTCAGGG GGCCACATAG TTCAAGGTCA CCTCGGAAGT TAGGAAGAGT 300
TCAGACTTGC CAGGGCCTCT AATTCTAATT CATGTATGTT TCCCAGGGCA GTGGACTGCA 360
CTGTGTTCTG AGCCTCTGGG CCACGCCCCC AGGCAGACTC CCCTCCCCGC AGCAGGCCAG 420
AGCCATTCTT GTAGTTCTCA AGTGCATTGG GGTAGACATT GGTTAAGCCC CTCGTGCCAG 480
CCAACTGCAG TGTAGCTTTA CCTGGTGCAC CTGCTGGGGA GCTGGGAGTT TCCACCACAG 540
GCTTCCCAGA TAGGATTTCT GTCAGCGGCT TTGACAGAAT GCCTCTGTCC ACACAGCCTC 600
CCCCACCCCA AGCAGCAGGT AATGGCTGAC ACTTAAATCA GGCAACTTTT AAACTTAACA 660
CCACTGAGAG GCCTTGAGTT GGGGACCAGA GGTTGCTCCT AAAGGCAGGG AGCAGGTTGA 720
AGGAGCCTCC GCTCTCTCTG AGCAGCCTGT GCTGTGCCCC ACGGCTGGTC ACGGCTCTGC 780
AAGAACCCAC CCAGAGTGAT TCAGAACAAC AGGTGGAGTC AGCGCTCGAT AGGAAAACTA 840
GATACCTGCT TGGCTCCAGG CCCTGGAGCG GAATGTGTCC ACGTACTGGG CGCTCATTCG 900
CTTGCCTTCC TCAGCACACG GTTTACCCTC CCTGAGCCAA GGCAGAGGAG AACCCAGGCC 960
CTCCATCAGC AGCTTTGCCT GCTGCCATCC ACCGTTTGCT CTTCTCCTAG TCAGGCTGCA 1020
CCCGTTTCTG GAAGCCAACT GCAGTCTCTT CTATGGAGAC AGCAGGCAGA CCTGGTCATC 1080
TCACACACAC CCTCTCATCT GACCCACACA CCACCCCAGA AGGGAGGGTG AGGACAACAG 1140
TGTTCCTCCC ATTTAACAGA TTAGGCCTCT GAGGCTGGGA GAAGAGGAGT GGCTTTCTCC 1200
AACTCATATG GCTGGTGCTG CTAATAAGAA AAGCCAACAT TACTGAGTGT TTATTCTGTG 1260
TCAAACGCTG TACTGAATGC TTTTTGTTGC CTCTCTTCGA CTTCACAGCA ACCTTATGTT 1320
GTTGTTACTG TTATTCCCCT CCCTTCACAG ATGTCAGAGA TATTTGATAA CTCGCCTGCT 1380
GAGGGATAGG ATTGAACCCA GGTCATATGA CTTCAAAGTG CACACACTTA ACCACCGTAC 1440
TGGTCTGCAC CCTTCTGTCT CCTAATCCAG TGCTCTTTGC CTTTTCCTTG CTGCCCTGTC 1500
AGAGAACCCC AGCTGGGGCC TCAAACCTGT CCCAGTCTGC CTCACTGTGT TGACTCCAGA 1560
TAGCCCAAGA GCAACCCAAC CTGCCTCATG GTGTTGGGCC GAGGCCAGTC ATAGCAGTGA 1620
GTGTTCTGGG GTCATGCAGA GGCAGCCCTC AACGATAGAA TAGACAGGCC CATTTTTAAA 1680
TCCATCAAAA GACCTCCAAG GCTCCCCACC CACTAGCCTG CCCTGACAGG AAACAGGTTG 1740
TTAAGAGTCT CAAATGTCAG GCCGTGGTGC TGTTTTGCAC AATTGCCATA GGCCAGCGCT 1800
CATTTACCCT GCCTTCCAGC TTCCCTCCCT CTGCCTTTTA AGCATAGATA TGTTGCCTAG 1860
AGCTTGGGCT GTTTCTGGAA AACAGAGTTG TTTTGGGAGT TAAATGAGCT TATTTAAGTC 1920
AAGCAGTTAG AACAGCACTT GACACTAGAT AAGGGCTTTG GAAGTGTTTG CTATTATAGC 1980
TGTACTTTCT ACTCTTTCTT TTCTTTTCTT TTTTTCTTTT TTTTTTCTTT TTTTTTTTTT 2040
TAGATGGAGT TTCACTCTTG TTGCCCAGGC TGGATTGCAA CGGTGCGATC TCGGTTCACA 2100
GCAACCTCCG CCTCCCGGGT TCAAGTGATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA 2160
TTACAGGCAT GTGCCACCAC ACCCAGCTAA TTTTTTGTAT TTTAATTAGA GACGGGGTTT 2220
CTCCATGTTG GTCAGGCTGG TCTCAACTCC CGACCTCAGG TGATCCACCC ACCTCGGCCT 2280
CCCAAGTGCT GGGATTACAG GTGTGAGACA CCACGCTCGG CCTGTACTTT CTACATTTTC 2340
TACAGGAGAC ATGTATTACT TGCAAGCTAA CATAATGAGG TACTTAGCAT AAGTTCTGTA 2400
GCCCCAGTGG GGATCTCTGA ACCAGGAAAA GGGTAACCCC CACAGCTGGG CACAGATGCC 2460
AGGAGAGGGA TGATTGAGGC ATGTCCGCTC CTCTCCTCTC CATCTAGGTC CCTACTAACA 2520
TGCCCCTTCC TCCACTTCCC CTCTTCTTTC 2550