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

TagContent
EnhancerAtlas ID
HS148-01685 
Organism
Homo sapiens 
Tissue/cell
NHLF 
Coordinate
chr1:223917700-223920530 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs140084787chr1223920445hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF2MA0051.1chr1:223919971-223919989GTAAAGTGAAAGCAAATT+6.52
ZNF263MA0528.1chr1:223919696-223919717GGAGAAAGAGAAGGAGGGGGC+6
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00224chr1:223917623-223923297Adipose_Nuclei
SE_01908chr1:223918292-223919960Aorta
SE_02306chr1:223918166-223920027Astrocytes
SE_04026chr1:223918327-223919959Brain_Anterior_Caudate
SE_05036chr1:223918296-223919826Brain_Cingulate_Gyrus
SE_05972chr1:223918153-223920025Brain_Hippocampus_Middle
SE_05972chr1:223920132-223922577Brain_Hippocampus_Middle
SE_07159chr1:223918575-223919801Brain_Hippocampus_Middle_150
SE_07159chr1:223920244-223923166Brain_Hippocampus_Middle_150
SE_09681chr1:223912826-223918041CD14
SE_09681chr1:223918139-223920041CD14
SE_23408chr1:223918840-223919937Colon_Crypt_1
SE_24051chr1:223918949-223919614Colon_Crypt_2
SE_25230chr1:223918779-223919775Colon_Crypt_3
SE_26209chr1:223918227-223919614Duodenum_Smooth_Muscle
SE_26925chr1:223918492-223919864Esophagus
SE_31491chr1:223918204-223920043Gastric
SE_31491chr1:223920239-223923646Gastric
SE_37129chr1:223917375-223920072HSMMtube
SE_38254chr1:223917692-223922239HUVEC
SE_38957chr1:223918328-223919928IMR90
SE_41495chr1:223918394-223920179Left_Ventricle
SE_42269chr1:223918111-223920107Lung
SE_42269chr1:223920225-223923100Lung
SE_44530chr1:223917549-223919989NHDF-Ad
SE_44904chr1:223918045-223919953NHLF
SE_45872chr1:223917531-223920254Osteoblasts
SE_49408chr1:223918777-223919926Right_Atrium
SE_50365chr1:223918695-223919952Sigmoid_Colon
SE_51879chr1:223918137-223919804Skeletal_Muscle_Myoblast
SE_53249chr1:223918717-223919906Small_Intestine
SE_55958chr1:223918085-223920003u87
SE_63671chr1:223918137-223919937HSMM
SE_65644chr1:223918515-223920092Pancreatic_islets
SE_67677chr1:223918085-223920003u87
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1223917746223917961
Number: 1             
IDChromosomeStartEnd
GH01I223730chr1223917704223922480
Enhancer Sequence
TCCCAAAAAA CCAAAAAAAA AAAAAAAAAA AAAAAAACGA AAACCTGAAA TCAGTTGAAA 60
AGTGTGCCTG GGTTGAGATA AGAAGTTGTT AGAGACCAAG GTTTTTATTA TGTAGATGAA 120
GTCTCACAGA GGGCCACTCT CAAAGGCAAT AGATGGCAAA TGTTTTCTAT TCAGACCTTT 180
AAAAGGTGCT ACTAGATGCT CAGCTAATCT CTTCAGGATC AGAAAAAGAC CTGAAGGGAA 240
GGTGATTCTC TACATCAAGC TTGTCCAACC CTCGTGCTGC CCAGGATGGC TTTGAATGTG 300
GCCCAACACA AATTTGTGAA CTTTCTCAAA ATATTATGAG ATTTTTTTTT TTTTTAGCTC 360
ATCATCTATC ATTAGTGTCA GTGTATTTTA TGTGTGGCCC AAGACAATTC TTCTTCTTCC 420
AGTGTGGCCC AGGGAAGCCA AAAGATTGGA CACCCCTGCT ATAGAATGTA GATTTTCCCA 480
CAAGAGACAG CTTTCAGAGA CATTTCAAAA TCTGTCAGAA AAATATATTT TGGGCTAAAA 540
TACTTTGATT TCTTTCAGGG CCTGCTATCT GTCATGTGAT GCTCTACTAG AGTGTGGTTG 600
GAATTTGGTA TCTTATTGCT AGGAAGAGTC TGTTTTGTGA GTCTTAAGAT CTCTGTTTTC 660
AGTTAAGGCT GGTCAGCTGT GCCTGAATTC CTAAAGGAGG AGGATAAAAT GAGGCATGAC 720
GGACCTCCCT TCCCATCGTG GCCTGAACTT GTTTTTCAGG TTTACCTTGG AATCCCCTTG 780
ACTAAGGGGG CACCCATTCA GTTAGTTAAG GGGCTTAGAC TTTGATTTTT AGTTTACAGT 840
AGGCTGAGGT GTATTAAATG CATTTTCGAC TTGCAATATT TTCAACTTCT GATGGATTTG 900
TTCAGATGTA ACCCCGTTGT AAGTTAAGGA GCATGTATAC TTGTATCTAA TCCACTTTGG 960
GCATTGCTGC CAGAAAACCT GTCCTCAGGG AGCTATGGAA GTAGTGGAGG CAAATTATTA 1020
AATGGATGGA TTAATTCCAA GTTCAGATCA TGTTGGGAGT CAGCTGGGAG TCAGTGTGAG 1080
GATCTGGGAG GGGAACAGTA AGGGGTTAAG AGAGATACCC CAAAGGATGA TTAAGGAGGG 1140
AGAGTTGGAA GGAAGGTTTC CCACAAAGAG GAAGCAGGGA GTGATTCATT CTGAAAAAGG 1200
CAAATATTTT ATTATGCTTG GAGGGTCTGG TGCAGAAGGG GAAAGGAAGA GAAGGAAGTT 1260
TGGCTTAAAT TCCCTTAGGA GCCAGTTCAG ATTCCTAAGC TGGCCCGGAC ATCCAACCCA 1320
ATCCGCCTAG CCCCAGCCCT CTCCAGTTCC CAATGCCCAG CCCCACAATG CCCGTCCTGC 1380
TGCCTGCCTG TTCTGGACTC TGCACTTGAC CTTCCCTCTC CCTGAAAGTG CCCCTGCTCT 1440
TCCTCACCCA GCTCCCCGCT CTAAGCCTTC CTCGCCCACC CCAGCCCTCC TACAGTCCCA 1500
GTCTGCCCTG TTCAGACTCA AAGCCTCATG CTCACCACCA TCATCCACAA CCAGTTTCCA 1560
CGTCTGTCTC CTGCCGGCTG TGAGCTCACT GCCTCAGAAC CAGCGCCAGT CTCCTCTAGA 1620
CTGAGTACAG GCCTGGCACG GAGCCAGGAA TGCACCAACA AGGAGCCTGA GACTAGATTG 1680
GAGGGGAAAG AGACATGTCC TCCAGAGTTG ACTTACGCGA GGACAGAGGT GTGCAGAGGC 1740
ACGGCAAGCT GGGCCCCAGG CGAGAAGCAT GGAGTGAGGG ATGTGGAGGC AGCGGAAGGC 1800
ATCTGGGAGT CTGGGCTGCC CCGTAGCAGC TCTGTGTTCT GCCTGCTCTT CCTCCAAGAT 1860
GAGCTCCCTT GGCCAGTGTG TGAAACGTGT GTGTGAGTGT GTCACCGGTA AGCTGAGTTC 1920
TTTCCCTACT TGGTATCAGT TGCAAAGAAA GAACACTCAG TTGGAAAAAA AGGCAAGAGG 1980
GTTTTATTCC TGACCAGGAG AAAGAGAAGG AGGGGGCTCT TGCTCTAAAG ACACCTTCAC 2040
CCCGAGCCAT GGAAACTGGG GAGTTGTAAG GAGATAGGTG TGGGGCAGGG AGGTGTGTAA 2100
GCAGGTGTGG GGTCACGGTG TGGGGGTGGA GACCTCTAGA CGCTCAGGCC CAGGTCATAA 2160
ACATGCCTCT CCATACAATG CAAGATGTGT TACCAGAAAG GGGTCCTGAT CTAGAACTAA 2220
GAAAGGGTTC TTGGATCCCG CTCAAGAAAG AATTCAGGGT GAGTCCATAC AGTAAAGTGA 2280
AAGCAAATTT ATTATGAAAA TAAAGGAATA AAAGAAAATC TACTTCATAG AGCAGCCCTG 2340
AGGGCTGATG ATTGCCCATT TTTATGGTTA TTTCTTGATT ATATGCTAAA CTTCTTGATT 2400
ATATGCTAAA CAAGGGGTGG ATTATTCATG CCTCCTCTTT TTAGATCACG TAGGGTAACT 2460
TCCTGATGTT GCCATGGCAT CTGTAAACTG TCATGGCTCT GGTGGGAGTG TAGCAGTGAG 2520
GACGAGCAGA GGTCACTCTT GTCACCATCT TGGTTTTGGT AGGTTTTGGC CGGCTTCTTT 2580
ACTGCAACTG TTTTATCAGC AAGGTCTTTA TGACCTGTAT CTTGTGCCGA CTTCCTATCT 2640
CATCCTGTGA CTTAGAATGC CTTAACTGTC TGGGAATGCA GCCCAGTAGG TCTCAGCCTC 2700
ATTTTACTCA GCTCTTATTC AAGATGGAGT TGCTCTAGTT CACACGCCTC TGACACATGT 2760
TCAGAAATAA TGGTGATTTT CTTCTACAGG TGGGGACGTT AGCATTATAA TGACATGGTA 2820
AAGTTCTGAA 2830