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

TagContent
EnhancerAtlas ID
HS113-00424 
Organism
Homo sapiens 
Tissue/cell
Keratinocyte 
Coordinate
chr1:17884650-17888480 
Target genes
Number: 6             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr1:17886449-17886460GGGTGACTCAG+6.02
JUNBMA0490.1chr1:17886449-17886460GGGTGACTCAG+6.02
ZEB1MA0103.3chr1:17885135-17885146GGGCAGGTGGG-6.14
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00612chr1:17885040-17898127Adipose_Nuclei
SE_01537chr1:17883748-17887179Aorta
SE_01537chr1:17887238-17903710Aorta
SE_03096chr1:17885238-17886505Bladder
SE_03096chr1:17886523-17887210Bladder
SE_03096chr1:17887277-17889743Bladder
SE_06186chr1:17884729-17903611Brain_Hippocampus_Middle
SE_23081chr1:17884927-17887129Colon_Crypt_1
SE_23081chr1:17887286-17888651Colon_Crypt_1
SE_23747chr1:17885515-17887093Colon_Crypt_2
SE_23747chr1:17887805-17888569Colon_Crypt_2
SE_24767chr1:17885691-17887095Colon_Crypt_3
SE_24767chr1:17887293-17888681Colon_Crypt_3
SE_26139chr1:17885349-17886817Duodenum_Smooth_Muscle
SE_26139chr1:17886970-17889235Duodenum_Smooth_Muscle
SE_26573chr1:17884636-17889887Esophagus
SE_28131chr1:17885813-17887223Fetal_Intestine
SE_29073chr1:17885548-17887452Fetal_Intestine_Large
SE_31687chr1:17884872-17887260Gastric
SE_31687chr1:17887279-17889702Gastric
SE_34117chr1:17885456-17889289HCC1954
SE_40808chr1:17884961-17889757Left_Ventricle
SE_43031chr1:17885865-17889757Lung
SE_46963chr1:17886184-17886643Ovary
SE_46963chr1:17887314-17888759Ovary
SE_47562chr1:17885148-17887191Pancreas
SE_47562chr1:17887302-17888795Pancreas
SE_50079chr1:17884800-17887187Sigmoid_Colon
SE_50079chr1:17887254-17888851Sigmoid_Colon
SE_52601chr1:17885107-17888827Small_Intestine
SE_54767chr1:17885171-17898261Stomach_Smooth_Muscle
SE_57000chr1:17885998-17886534VACO_400
SE_57000chr1:17887871-17888648VACO_400
SE_65277chr1:17884558-17889999Pancreatic_islets
SE_68684chr1:17884738-17887162H9
SE_68684chr1:17887236-17888637H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11788493917886084
Number: 1             
IDChromosomeStartEnd
GH01I017558chr11788516117889539
Enhancer Sequence
TCCATCCATC TATGCATCCA TCCATCCATC CACCCATCCA TCCATCCATC CATCCATCCG 60
CCTGCCCATC CATTCATCCA TTTATCTACC CATCCACCTA CTCATTCATT CATCTATCCA 120
TCCACCCACC CGCCCATTTA TTCACCCACT CATCCACCCA TCATCTCTTG AATCTCTTCG 180
GCATGCTAAG GACTGCCCTG GGTATTGGAG AGACAGAAAT GAAAGGCATT ATTCTTGCCT 240
TCAAGGAACT CACAGTCTAG TGGGCTGTCA GAAAACTAAG CAAATGATTC CAGTCCAGAG 300
TGTTAGGTGC CCAGAGGGAC AAGTGGCCAG CTGTCTGTCC CAGTGGTCAT CATGGGAGAC 360
TGCTCTGATG CCAGCTGCAT GTGCTAAGCA AAGTGTATTT GGGAGTGGCC CAGGCAGATG 420
AGGTGGGGAA TGGCTTTCAG GCCCTGGAAG GGTCTTGCCT TTGGGAAGGC AGGTCATCGT 480
GGCTGGGGCA GGTGGGGACC TTTTCCTCTT TTGACACTCA GGTTCTCTTT GGTTTTGCAA 540
GTGGTCCCAC GAGGTCTGGG CCTCAGTAGA TGCTTAGCCA ACATGAGTTG TCAGTGAATG 600
GGGAGATGAG TCAGAAAGGA TGCCCTGTGA ACCTCACTGA GGAGCTGTGG CTCTGTGGGG 660
CCACAGATAG GGTCCAGGCA GGGGACAACA CTGTGCCACA GGCTCCCTGG GCTGGGCAGG 720
GAGAATGGTG GGGAGGGCTG AGGGGCCCTT CCCCAGCTTC CTCGGCTTTC AGCTCTTTTC 780
TTGTGTAGAT TGGAGCCTTT GCATTCATGA AAGCTGATGA CTCCTTTCCA CCAGTGAATT 840
TCCTGCAACC CACAGGGCCC GGCCTCAGTT GGGGTGTGGG GGGAGCAGAA TGATGTGGGG 900
AGAGTGGTGG ATGCTGTGGC AGCTAAGAGC CTTGGCCTCC GGAATCAGAC TGCCTGATGT 960
GGGAGTCTTA CTTCTGCCAT TTGTCAGCTG TGTGTCCTGG GGCAAGTGTC TCAACCTTTC 1020
TGTTTCAGTT CAGTTATTCA GTTGGGGATA ATATCAGTCC CTATCTCATA TGGCTGTTGG 1080
GACGATTAGG AGTTATTTCT GGTAAAGCAC TTAGTGCAAT CCTGGTACAT GGTAAGTATC 1140
GACACAAGGC AGCTTCGGTG TGGAGCTTTG GAGGCAGCCC TGTCACAGGG GCGGGACACT 1200
AGAAGGGGCT GGGTATTTAT TAGCCTTGGA GCCAGAAGAC CTGCTTGGAA TCCCACCCCT 1260
ACCTCTGACT GATTGTAGAG ACCTTGGCAG GCTGATTCAA TGCTCTGAGC TCAGATTTGT 1320
CATCTGTGAA TAGGGGACCG ACACCCCCCA GGGCCGCTGG GAGGAGTCAC TGGGTCTGAT 1380
GGCTCATTCT CTGCATTGGG CTTATGATTG AGGTAGGAAA ACTCTAAACA GGAGGAGTGA 1440
AATCTTCATT TGCTAGGGTG GCCTGGATGG CCATGCCTGG GGGTCAGTCT GTGGGGTCTG 1500
TAGGGCCACC TCTCTTGGCC CTGGCCTTTT CCCTTAGTTG CCCTCACTGT TGCAGGTTCC 1560
TAAGGAAAGG GACCGTCATG TGACTGGGGC CCAGGGTCTT CAGAACAAGG TGCTACAGGG 1620
GCAGAGGGTC AGGCTGGTGC CATTTCATTT GCAGGAGTGC TGGGGAGGGT GACTGTCCTC 1680
CTCCAGCCAC ACTGGGTCTG GGTGCCTGGG AGAGACTGAG GTTTCTGGTG CCTGCCCTGG 1740
GTTCAGCACT CCTGTCCCTC CACACCTCAT GTTCCTGCTT GATTTGAATT CTCAGGGTTG 1800
GGTGACTCAG GCATGCCTGA TGCCCTGCAA GATTTGGTTC ACAAGCAGGT AAATATTAAC 1860
CCACACGCAT AGCTCCAAAT GCAAACCTGT TTGGGCTGGC TTCTTGGGGG ACAGCTAGGC 1920
TCCGAGTGTC CCCCTCTTCC CCCAGCTGAT GGCCAAGGTA AGCAGGTGCC CTCCAGGGGA 1980
ACGAGGTCAC CTGCTTTGTG CCAGGTGATT GTACTGAATT CGCACCACTG TCCGGGGGCA 2040
GGGGCTGCTG TATCTATTTT ACAGCAGAGG AGGAAACCAA GACATCAGGA GGAGGCCAGC 2100
TCGGTTTACA CAGTTAATGA GAAATGGGCC TATGGCTAGA ACCCAGGAGT GCCTCCCTGC 2160
AAAGTCCACA CTTTCCCCAC CTGGATCTCC AGCTGTCTCC TTGCTGTTAG GGTCACAAGG 2220
CAATGCTATG TGTATCAGAG GCACCTGAGG TTTGCTTTCT GGCTCCACTT TGCCTGGGCC 2280
TCAAATGCCC CTTTTGTGAA GTGGGGCCAG GCTGGTTTGG GGTCCCTGAT AGGCAGGAAC 2340
CAGCCCAGGA CACTTGAGTG CAGTAATGGG GCCTGGGCTT GGATTTGGGA GTAACCACCT 2400
GGCCAGCCAA ACAACGATCT TTTTTTTGAG ACGGAGTTTC ACTCTTGTTG CCCAGGCTGG 2460
AGTACAATGG CGCAATCTCG GCTCACCACA ACCTCTGCCT TCTGGGTTCA ATAGATTTTC 2520
CTGCTTCAGC CTCCTGAATA GCTGGGATTA CAGGCATGCA CCACCACACC CAGCTAATTT 2580
TGTATTTTTA GTAGAGGTGG GGTTTCTCCA TGTTGGTCAG GCTGGTCTCG AACTCCTGAT 2640
CTCAGGTGAT CTGCCCACCT TGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACTG 2700
CGCCTGGCCC TCAAGCATCT CTTGAAGACC TGCCAGGAGG CACTGTGGGG ACACCCAGGG 2760
AGGAGCCACA GTTTCTGTCC TCTGGGAGCT GACACGTGAG CAAGAGTGAG AACACAGGTT 2820
TAGGGGCTCC AGGACTGGGT TTGAATCTTG GGTCTTAGTA GCTGTGTGGT CTTGGGCAGG 2880
TGCCTTTGCC TTGCTCAGCC TTTGGGGCTC CCTCCAAAGA TGGGAATAAC AAGCCTTACT 2940
TCAGAGTGCA TTGTGAGGCT AAAGTGAGAT GGTGTCTGCA AAGCTCCCAG CACGTAGTAG 3000
GTGCTCAGTA AGGTGGTTTC CCCTGCCCAG AACCTCAGAT GACTGTCTTC TAAGTCTGAG 3060
AGCAACCAGT GGGCCTCAAA GGCGATTGAG GGCTGCTTCC CCTGCCCTGC ACCTCCCCCC 3120
CGCCCCGTCA TGCTGGCAGC CCGGGAGCAG TCTCTCACGG TTCTGTGGGC AGCTGGAGAT 3180
GGGGCAGAAG CGGGCGTCAG CTCCACAGTG GGGGCACTGG GAGGTGGGGC CAGGCTTGAC 3240
TGGGAGGAGA GGGAGATGCT GGCTTTTCCT TGGTCCTGCC CCCCGCAGCC TTGCAGTCAG 3300
AGGCAGCCCC AATGAGCCCT CTGCAGTTCT GAGTGCCTTC CTCTCCTGTC TCGCAGAGGG 3360
GGAGCCTCAC AAACCCTGAC AGCAGAAGTG ACTTGCCCAG CGTCGATGGG CGCTGGTGGC 3420
AGAGCCAGGC TGACCCCCAG CCTGAGGCCC ACCCGATCCC GATGCTGCAC TCCTAGCTCC 3480
TTGGCGTAGG TCCCTGGGGC TGTCGGGTGC CCTGGCCTCC CTGGCCTGCC CTGGAGCCAG 3540
CTATGAAGGA ATATTCTGGG GCACATGACT CACAAGGCTG GCCCTTCCAC TTTTTGTTTT 3600
CCTTTCTTTT ACTTTTCCCT AATACGGTCT CCTGTGGCCC TTGCTTCTCC TTTCTTGGGG 3660
CTCTGAGATG GCAGTGCCTT TTGCCCTGGA AAGCCTGTCC TGGCAGAGCT CCTGTTAGCT 3720
GTCGACCACA GCTGCTCAAT CGGGAAGGTT CCAAGGGAGG CCGAGCAAAG GCATCAGAGC 3780
TGCACAGACC TGGGCCATAG CTTGGCTGAC CTACTCCCTA GCTATGTGAC 3830