EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-03466 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr1:223925830-223928060 
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: 1             
ChromosomeStartEnd
chr1223926096223927104
Number: 1             
IDChromosomeStartEnd
GH01I223736chr1223924574223930136
Enhancer Sequence
GTTCAAAAAC AATTTTTAAT CTTATTACCT TTTTTTTTCT TTTTTGTGAG ACGGGGTCTT 60
GTTCTGTCAC CCAGGCTGGA GTACAGTGGT ACAATCATAG CTCACTGCAG CCTTGACCTC 120
CCAGGTTCAA AGTGATTCTC CTGCCTCAGC CTCCCAAGTT GCTGGGACGA TAGAAGCATG 180
ACACCACACC TGGCTAATTT TTTAAAAATA ATTTTTATAG AGACAGGGTC TCACAGTATA 240
GTGAGATTTC AGGGTGGTCT TGAAATCCTG AGGGCTCAAG AAATCCTCCA GCCCTGGCCT 300
CCCAAGAGCT AGAATTACAG GCATGAGCCA CCGTACCTAG CCCTATTGCT ATTTTTATTA 360
GCATTACATT AAGTTTATAG GCTAACTTAA GAGGACATGG CATTTTTATG ATAATGAGTT 420
TTTGCAGTCA AGAACGCAGG CCAGTTTTTT TTAAATGGGG TAAATGATTG TCCAAGCGCC 480
TCCAGGCAGG CTCACGTGCA CACTCTGGAG TCAGTGAAGA AGGTGAACAG CTGACAGGAG 540
CAGCCTCCCA GTCAGAGAAG CCCTGCACAC TGTTGCAAAC AGACAGCTTG CATCTGGAGT 600
CTTCTGTGAT CCGAGGAGGA AGCGTGGCTG AGTCCTTCCC AGAAGAGGGT CTGGAGCTGT 660
GAGTTGGGGA CAATTGTCAG ATTCTAGCAG TGAAAGTGGT TCATGTGCAG GTGCAACCTG 720
CCCCGCAGTC ACGGGACACA GCCACATGGA GCCGAGCCAC GCTCTCAGAG AAGGAGCCAG 780
GGAAGAAACA CCCTAACTGC ACTCCTCCCT TCTTCTGGCC CCCAGCAGCC ATAGGCCCTG 840
GGCCCCCGGT GAGATACCCA TAGAGATCAG CTCCCAGGCA GCAGGATGGA GGGTGTAGAC 900
TGGACATGAA GAGGCAGCTG GAATGTATCG GGCACTCAGC TCCAGCTCAC CACGATCCAG 960
GCACTCAAGT TCCCAAGACA ATAGTTTCTG CTCTCAGATA AATGGAATAA TTAAGGATCA 1020
AAAGGTTATC AACAGGTAAC CAAGCATAAA CAGATTTTTT TTTTTTTTTT TTTTAGACAG 1080
AGTCTCACTC TGTGCCCCAG GCTGGAATGC AGTGGTGCAA TCTGGGCTCA CTGCAACCTC 1140
CACCTCCCAG GTTCAAGTGA TTCTCATGCC TCAGCCTCTC CAGTAGCTGG GACTACAGGC 1200
GCGTGCCAAC ATGCCTGGCT AATTTTTGTA TTTTTAGTAA AGATGGAGTT TCACCATGTT 1260
GGCCAGGCTA GTCTTGAACT CCTGACCTCA TGTGATCTGC CCACCTCGGC CTCCCAAAGT 1320
GATGGGATTA CAGGTGTGAG TCACCATGCC TGGCCCATAA GCAGATTTTG TACCTGAGCA 1380
GGAAGGCTAA GAGCTTGTAA CAACTGAACA TTCCCCCCGG AGAGGAAGGC AGGAGTTTTG 1440
CTTGTGCCAA GTGCACTGTT CAGACAGTCC TCTGAGGTAC ACCAAGGTCT GAGTAGCCAT 1500
CCCACCCTCC CCTCTGCCAA AATTTTTGTG TGACTGGAGA GCAGAGCCCT CCTCCAAAAA 1560
TAAAATGAGC ACAAGGAAAA TACTATTTGC AGATACATAA TATTAAAACC ATAGGTCTTT 1620
CTTTTTCTAG TCCCATCCAT ATGGCAACAT TCCAGGAGAG GCCTCCGTCA CTGGAAGGCA 1680
CCCTCAGGGG CTTTCCTGGA GCTAAAAACA GTTTAAGCCA AAAGTTATTT GTAGCATCTG 1740
AGTTAAACTC TTCGTCTCAC CCTTCTCGAG CTAGCTGGCT TATTTTATCC GGACCAGGAT 1800
ATAACAGCTC TAAACAGGCT TTGCCAGGAA GAGACGTCAT GGACTTCAAC CAGGGCACCT 1860
GACCAGGAAG AAATCACTGC AGGATGATCT GAAAGAGTTT TCATAAATTA TTTTACGTAA 1920
GGTAGATTCT GACCTTGATG GGGACAGCCA AGGTTCTGGA CCCTCAGCTG GGAAAGATGG 1980
GACTAAGTCT ACAACTGCTG AGGTTGTAGA ACAGGCTTCT TGTTGGGAGG AACCCTCTTG 2040
TGGACATGGG CCGTCGAGGT GGAGTGAGAG AACACCGTGC CACCTGGACG CTGAAACACC 2100
ATTGAGTCAC CTCTGTTTGA AATGCTTGTT CCCTGGTGCC GTAAAGAAAT AGCACTTGAA 2160
CATAAATTTA ATTTACTCAG CAAGGACATT TTTATACTTT CTGTGAAAGG GTACACTCAC 2220
CAGGAGTTTT 2230