EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS178-02290 
Organism
Homo sapiens 
Tissue/cell
Skeletal_muscle 
Coordinate
chr1:223926090-223928380 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GFI1MA0038.2chr1:223927699-223927711GAAATCACTGCA+6.74
Nkx2-5(var.2)MA0503.1chr1:223926788-223926799AGGCACTCAAG+6.14
Nr2f6(var.2)MA0728.1chr1:223927104-223927119TGAACTCCTGACCTC-6.22
RORAMA0071.1chr1:223927759-223927769TGACCTTGAT-6.02
STAT3MA0144.2chr1:223926464-223926475CTTCCCAGAAG-6.14
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00224chr1:223925520-223928901Adipose_Nuclei
SE_01908chr1:223926095-223926935Aorta
SE_01908chr1:223927075-223928148Aorta
SE_09681chr1:223926086-223926867CD14
SE_23408chr1:223925806-223926930Colon_Crypt_1
SE_23408chr1:223927008-223928133Colon_Crypt_1
SE_24051chr1:223926231-223926878Colon_Crypt_2
SE_24051chr1:223927084-223928100Colon_Crypt_2
SE_25230chr1:223926296-223926903Colon_Crypt_3
SE_25230chr1:223927114-223928239Colon_Crypt_3
SE_26209chr1:223926103-223928290Duodenum_Smooth_Muscle
SE_26925chr1:223926095-223928145Esophagus
SE_31491chr1:223923671-223928232Gastric
SE_33950chr1:223925357-223926983HCC1954
SE_33950chr1:223927048-223928269HCC1954
SE_34545chr1:223926186-223927072HCT-116
SE_36294chr1:223927044-223927974HMEC
SE_37129chr1:223924560-223926499HSMMtube
SE_37129chr1:223926584-223928521HSMMtube
SE_41495chr1:223927102-223928062Left_Ventricle
SE_42269chr1:223925796-223927012Lung
SE_42269chr1:223927049-223928176Lung
SE_50365chr1:223925795-223926977Sigmoid_Colon
SE_50365chr1:223927008-223928158Sigmoid_Colon
SE_53249chr1:223926157-223926979Small_Intestine
SE_53249chr1:223927086-223928250Small_Intestine
SE_64794chr1:223926064-223928210NHEK
SE_65644chr1:223925909-223927309Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1223926096223927104
chr1223927976223928193
Number: 1             
IDChromosomeStartEnd
GH01I223736chr1223924574223930136
Enhancer Sequence
TGAAATCCTG AGGGCTCAAG AAATCCTCCA GCCCTGGCCT CCCAAGAGCT AGAATTACAG 60
GCATGAGCCA CCGTACCTAG CCCTATTGCT ATTTTTATTA GCATTACATT AAGTTTATAG 120
GCTAACTTAA GAGGACATGG CATTTTTATG ATAATGAGTT TTTGCAGTCA AGAACGCAGG 180
CCAGTTTTTT TTAAATGGGG TAAATGATTG TCCAAGCGCC TCCAGGCAGG CTCACGTGCA 240
CACTCTGGAG TCAGTGAAGA AGGTGAACAG CTGACAGGAG CAGCCTCCCA GTCAGAGAAG 300
CCCTGCACAC TGTTGCAAAC AGACAGCTTG CATCTGGAGT CTTCTGTGAT CCGAGGAGGA 360
AGCGTGGCTG AGTCCTTCCC AGAAGAGGGT CTGGAGCTGT GAGTTGGGGA CAATTGTCAG 420
ATTCTAGCAG TGAAAGTGGT TCATGTGCAG GTGCAACCTG CCCCGCAGTC ACGGGACACA 480
GCCACATGGA GCCGAGCCAC GCTCTCAGAG AAGGAGCCAG GGAAGAAACA CCCTAACTGC 540
ACTCCTCCCT TCTTCTGGCC CCCAGCAGCC ATAGGCCCTG GGCCCCCGGT GAGATACCCA 600
TAGAGATCAG CTCCCAGGCA GCAGGATGGA GGGTGTAGAC TGGACATGAA GAGGCAGCTG 660
GAATGTATCG GGCACTCAGC TCCAGCTCAC CACGATCCAG GCACTCAAGT TCCCAAGACA 720
ATAGTTTCTG CTCTCAGATA AATGGAATAA TTAAGGATCA AAAGGTTATC AACAGGTAAC 780
CAAGCATAAA CAGATTTTTT TTTTTTTTTT TTTTAGACAG AGTCTCACTC TGTGCCCCAG 840
GCTGGAATGC AGTGGTGCAA TCTGGGCTCA CTGCAACCTC CACCTCCCAG GTTCAAGTGA 900
TTCTCATGCC TCAGCCTCTC CAGTAGCTGG GACTACAGGC GCGTGCCAAC ATGCCTGGCT 960
AATTTTTGTA TTTTTAGTAA AGATGGAGTT TCACCATGTT GGCCAGGCTA GTCTTGAACT 1020
CCTGACCTCA TGTGATCTGC CCACCTCGGC CTCCCAAAGT GATGGGATTA CAGGTGTGAG 1080
TCACCATGCC TGGCCCATAA GCAGATTTTG TACCTGAGCA GGAAGGCTAA GAGCTTGTAA 1140
CAACTGAACA TTCCCCCCGG AGAGGAAGGC AGGAGTTTTG CTTGTGCCAA GTGCACTGTT 1200
CAGACAGTCC TCTGAGGTAC ACCAAGGTCT GAGTAGCCAT CCCACCCTCC CCTCTGCCAA 1260
AATTTTTGTG TGACTGGAGA GCAGAGCCCT CCTCCAAAAA TAAAATGAGC ACAAGGAAAA 1320
TACTATTTGC AGATACATAA TATTAAAACC ATAGGTCTTT CTTTTTCTAG TCCCATCCAT 1380
ATGGCAACAT TCCAGGAGAG GCCTCCGTCA CTGGAAGGCA CCCTCAGGGG CTTTCCTGGA 1440
GCTAAAAACA GTTTAAGCCA AAAGTTATTT GTAGCATCTG AGTTAAACTC TTCGTCTCAC 1500
CCTTCTCGAG CTAGCTGGCT TATTTTATCC GGACCAGGAT ATAACAGCTC TAAACAGGCT 1560
TTGCCAGGAA GAGACGTCAT GGACTTCAAC CAGGGCACCT GACCAGGAAG AAATCACTGC 1620
AGGATGATCT GAAAGAGTTT TCATAAATTA TTTTACGTAA GGTAGATTCT GACCTTGATG 1680
GGGACAGCCA AGGTTCTGGA CCCTCAGCTG GGAAAGATGG GACTAAGTCT ACAACTGCTG 1740
AGGTTGTAGA ACAGGCTTCT TGTTGGGAGG AACCCTCTTG TGGACATGGG CCGTCGAGGT 1800
GGAGTGAGAG AACACCGTGC CACCTGGACG CTGAAACACC ATTGAGTCAC CTCTGTTTGA 1860
AATGCTTGTT CCCTGGTGCC GTAAAGAAAT AGCACTTGAA CATAAATTTA ATTTACTCAG 1920
CAAGGACATT TTTATACTTT CTGTGAAAGG GTACACTCAC CAGGAGTTTT GCCACGAGAG 1980
TACACCAAAC AAAGGAGACA GGGTCATTTA TAACCTGACG CGTCCACCCT ACTGCTGTGT 2040
CCAGTTTCCA TTGGCTGGAA CAGGACCTCC CATTCTGTAT TTGTCCCGAT TGGCTAACAA 2100
CTTAGAACTT TTTAAAAGAG GCAAAGGCAG AGGAGAACAA AGGAAGGAGG AAGTAACTTG 2160
TGGAATGCTG AGAAAGGTAA AAACACCTTT AGATAAGGAA GAGGAACAGG CTATGACCTA 2220
ATGCTTGCTT GGACCAGTAT AAGCATGCCA GGGAAAATAC TTAGGCTAAA TTGTGGGAGC 2280
TAAGAACATA 2290