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

TagContent
EnhancerAtlas ID
HS050-06002 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:223925860-223929000 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GFI1MA0038.2chr1:223927699-223927711GAAATCACTGCA+6.74
LHX6MA0658.1chr1:223928663-223928673ACTAATTAGC+6.02
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: 39             
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_23408chr1:223928467-223929077Colon_Crypt_1
SE_24051chr1:223926231-223926878Colon_Crypt_2
SE_24051chr1:223927084-223928100Colon_Crypt_2
SE_24051chr1:223928484-223928893Colon_Crypt_2
SE_25230chr1:223926296-223926903Colon_Crypt_3
SE_25230chr1:223927114-223928239Colon_Crypt_3
SE_25230chr1:223928443-223929149Colon_Crypt_3
SE_26209chr1:223926103-223928290Duodenum_Smooth_Muscle
SE_26925chr1:223926095-223928145Esophagus
SE_26925chr1:223928405-223929121Esophagus
SE_31491chr1:223923671-223928232Gastric
SE_31491chr1:223928466-223930048Gastric
SE_33950chr1:223925357-223926983HCC1954
SE_33950chr1:223927048-223928269HCC1954
SE_33950chr1:223928379-223929152HCC1954
SE_34545chr1:223926186-223927072HCT-116
SE_36294chr1:223927044-223927974HMEC
SE_37129chr1:223924560-223926499HSMMtube
SE_37129chr1:223926584-223928521HSMMtube
SE_38254chr1:223928343-223932514HUVEC
SE_41495chr1:223927102-223928062Left_Ventricle
SE_42269chr1:223925796-223927012Lung
SE_42269chr1:223927049-223928176Lung
SE_42269chr1:223928490-223929116Lung
SE_50365chr1:223925795-223926977Sigmoid_Colon
SE_50365chr1:223927008-223928158Sigmoid_Colon
SE_50365chr1:223928472-223929111Sigmoid_Colon
SE_53249chr1:223926157-223926979Small_Intestine
SE_53249chr1:223927086-223928250Small_Intestine
SE_53249chr1:223928478-223929116Small_Intestine
SE_64794chr1:223926064-223928210NHEK
SE_64794chr1:223928353-223929132NHEK
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
TTTTTTTTCT TTTTTGTGAG ACGGGGTCTT GTTCTGTCAC CCAGGCTGGA GTACAGTGGT 60
ACAATCATAG CTCACTGCAG CCTTGACCTC CCAGGTTCAA AGTGATTCTC CTGCCTCAGC 120
CTCCCAAGTT GCTGGGACGA TAGAAGCATG ACACCACACC TGGCTAATTT TTTAAAAATA 180
ATTTTTATAG AGACAGGGTC TCACAGTATA GTGAGATTTC AGGGTGGTCT TGAAATCCTG 240
AGGGCTCAAG AAATCCTCCA GCCCTGGCCT CCCAAGAGCT AGAATTACAG GCATGAGCCA 300
CCGTACCTAG CCCTATTGCT ATTTTTATTA GCATTACATT AAGTTTATAG GCTAACTTAA 360
GAGGACATGG CATTTTTATG ATAATGAGTT TTTGCAGTCA AGAACGCAGG CCAGTTTTTT 420
TTAAATGGGG TAAATGATTG TCCAAGCGCC TCCAGGCAGG CTCACGTGCA CACTCTGGAG 480
TCAGTGAAGA AGGTGAACAG CTGACAGGAG CAGCCTCCCA GTCAGAGAAG CCCTGCACAC 540
TGTTGCAAAC AGACAGCTTG CATCTGGAGT CTTCTGTGAT CCGAGGAGGA AGCGTGGCTG 600
AGTCCTTCCC AGAAGAGGGT CTGGAGCTGT GAGTTGGGGA CAATTGTCAG ATTCTAGCAG 660
TGAAAGTGGT TCATGTGCAG GTGCAACCTG CCCCGCAGTC ACGGGACACA GCCACATGGA 720
GCCGAGCCAC GCTCTCAGAG AAGGAGCCAG GGAAGAAACA CCCTAACTGC ACTCCTCCCT 780
TCTTCTGGCC CCCAGCAGCC ATAGGCCCTG GGCCCCCGGT GAGATACCCA TAGAGATCAG 840
CTCCCAGGCA GCAGGATGGA GGGTGTAGAC TGGACATGAA GAGGCAGCTG GAATGTATCG 900
GGCACTCAGC TCCAGCTCAC CACGATCCAG GCACTCAAGT TCCCAAGACA ATAGTTTCTG 960
CTCTCAGATA AATGGAATAA TTAAGGATCA AAAGGTTATC AACAGGTAAC CAAGCATAAA 1020
CAGATTTTTT TTTTTTTTTT TTTTAGACAG AGTCTCACTC TGTGCCCCAG GCTGGAATGC 1080
AGTGGTGCAA TCTGGGCTCA CTGCAACCTC CACCTCCCAG GTTCAAGTGA TTCTCATGCC 1140
TCAGCCTCTC CAGTAGCTGG GACTACAGGC GCGTGCCAAC ATGCCTGGCT AATTTTTGTA 1200
TTTTTAGTAA AGATGGAGTT TCACCATGTT GGCCAGGCTA GTCTTGAACT CCTGACCTCA 1260
TGTGATCTGC CCACCTCGGC CTCCCAAAGT GATGGGATTA CAGGTGTGAG TCACCATGCC 1320
TGGCCCATAA GCAGATTTTG TACCTGAGCA GGAAGGCTAA GAGCTTGTAA CAACTGAACA 1380
TTCCCCCCGG AGAGGAAGGC AGGAGTTTTG CTTGTGCCAA GTGCACTGTT CAGACAGTCC 1440
TCTGAGGTAC ACCAAGGTCT GAGTAGCCAT CCCACCCTCC CCTCTGCCAA AATTTTTGTG 1500
TGACTGGAGA GCAGAGCCCT CCTCCAAAAA TAAAATGAGC ACAAGGAAAA TACTATTTGC 1560
AGATACATAA TATTAAAACC ATAGGTCTTT CTTTTTCTAG TCCCATCCAT ATGGCAACAT 1620
TCCAGGAGAG GCCTCCGTCA CTGGAAGGCA CCCTCAGGGG CTTTCCTGGA GCTAAAAACA 1680
GTTTAAGCCA AAAGTTATTT GTAGCATCTG AGTTAAACTC TTCGTCTCAC CCTTCTCGAG 1740
CTAGCTGGCT TATTTTATCC GGACCAGGAT ATAACAGCTC TAAACAGGCT TTGCCAGGAA 1800
GAGACGTCAT GGACTTCAAC CAGGGCACCT GACCAGGAAG AAATCACTGC AGGATGATCT 1860
GAAAGAGTTT TCATAAATTA TTTTACGTAA GGTAGATTCT GACCTTGATG GGGACAGCCA 1920
AGGTTCTGGA CCCTCAGCTG GGAAAGATGG GACTAAGTCT ACAACTGCTG AGGTTGTAGA 1980
ACAGGCTTCT TGTTGGGAGG AACCCTCTTG TGGACATGGG CCGTCGAGGT GGAGTGAGAG 2040
AACACCGTGC CACCTGGACG CTGAAACACC ATTGAGTCAC CTCTGTTTGA AATGCTTGTT 2100
CCCTGGTGCC GTAAAGAAAT AGCACTTGAA CATAAATTTA ATTTACTCAG CAAGGACATT 2160
TTTATACTTT CTGTGAAAGG GTACACTCAC CAGGAGTTTT GCCACGAGAG TACACCAAAC 2220
AAAGGAGACA GGGTCATTTA TAACCTGACG CGTCCACCCT ACTGCTGTGT CCAGTTTCCA 2280
TTGGCTGGAA CAGGACCTCC CATTCTGTAT TTGTCCCGAT TGGCTAACAA CTTAGAACTT 2340
TTTAAAAGAG GCAAAGGCAG AGGAGAACAA AGGAAGGAGG AAGTAACTTG TGGAATGCTG 2400
AGAAAGGTAA AAACACCTTT AGATAAGGAA GAGGAACAGG CTATGACCTA ATGCTTGCTT 2460
GGACCAGTAT AAGCATGCCA GGGAAAATAC TTAGGCTAAA TTGTGGGAGC TAAGAACATA 2520
AAGTACATTG ATTTCTTTAT CATGGCTAGC AGATATTTAA GAATGTTAGC ACAGGTCTTT 2580
GAATAAATTT TGCTTCTAAG AGAAGTTACT ATTTATTCCT AATTAAATGG GGAGGAAGGT 2640
CTTTGAAGAG AAACCTTTAC ACCTCTTAAG GACAAAAGTC CCCAAGACCT GTCCAATTTC 2700
GAATTCAATT AGGTGAATTC GAAATTGACA CCAGCCTCTT TGCAGAGGAG ACTGTTTTGG 2760
TTATACATCA AAAGCCTGTG CTTTGCAGAT AGACCTGACA GCCACTAATT AGCTAGGAGC 2820
GTTGGGTGAT CCAGTCCACC TCCTTAAACC TCAGTTTCCT CAACTATGAA ATAGAATGAA 2880
AATAGTACCT ACCTTGGAAC TGTTCTGTGA CAAGGAAATG AGATAACATG ATAATGTGCA 2940
TAAGGCTTTT AGCTCGGGGC CTGGCACACC TAAGCCTTTG TGTAATCATT GTGTAGATCT 3000
TGTCACTGAG AACGCTTACA CGAGCAGATA TTAAAATAAA GGAAAGAAGT CAGTTGGGTA 3060
AGGGAGCTTC CCAGCTTGGT TCAAAATATT TTGCTGATTG GGGTGAGGGA AAGAGTGAAG 3120
GAACCAGAAG CAAAAAAAGT 3140