EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-00879 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:17885620-17888850 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr1:17886449-17886460GGGTGACTCAG+6.02
JUNBMA0490.1chr1:17886449-17886460GGGTGACTCAG+6.02
Number of super-enhancer constituents: 38             
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_23747chr1:17887310-17887685Colon_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_46963chr1:17886662-17887004Ovary
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
Number: 1             
IDChromosomeStartEnd
GH01I017558chr11788516117889539
Enhancer Sequence
CTTCTGCCAT TTGTCAGCTG TGTGTCCTGG GGCAAGTGTC TCAACCTTTC TGTTTCAGTT 60
CAGTTATTCA GTTGGGGATA ATATCAGTCC CTATCTCATA TGGCTGTTGG GACGATTAGG 120
AGTTATTTCT GGTAAAGCAC TTAGTGCAAT CCTGGTACAT GGTAAGTATC GACACAAGGC 180
AGCTTCGGTG TGGAGCTTTG GAGGCAGCCC TGTCACAGGG GCGGGACACT AGAAGGGGCT 240
GGGTATTTAT TAGCCTTGGA GCCAGAAGAC CTGCTTGGAA TCCCACCCCT ACCTCTGACT 300
GATTGTAGAG ACCTTGGCAG GCTGATTCAA TGCTCTGAGC TCAGATTTGT CATCTGTGAA 360
TAGGGGACCG ACACCCCCCA GGGCCGCTGG GAGGAGTCAC TGGGTCTGAT GGCTCATTCT 420
CTGCATTGGG CTTATGATTG AGGTAGGAAA ACTCTAAACA GGAGGAGTGA AATCTTCATT 480
TGCTAGGGTG GCCTGGATGG CCATGCCTGG GGGTCAGTCT GTGGGGTCTG TAGGGCCACC 540
TCTCTTGGCC CTGGCCTTTT CCCTTAGTTG CCCTCACTGT TGCAGGTTCC TAAGGAAAGG 600
GACCGTCATG TGACTGGGGC CCAGGGTCTT CAGAACAAGG TGCTACAGGG GCAGAGGGTC 660
AGGCTGGTGC CATTTCATTT GCAGGAGTGC TGGGGAGGGT GACTGTCCTC CTCCAGCCAC 720
ACTGGGTCTG GGTGCCTGGG AGAGACTGAG GTTTCTGGTG CCTGCCCTGG GTTCAGCACT 780
CCTGTCCCTC CACACCTCAT GTTCCTGCTT GATTTGAATT CTCAGGGTTG GGTGACTCAG 840
GCATGCCTGA TGCCCTGCAA GATTTGGTTC ACAAGCAGGT AAATATTAAC CCACACGCAT 900
AGCTCCAAAT GCAAACCTGT TTGGGCTGGC TTCTTGGGGG ACAGCTAGGC TCCGAGTGTC 960
CCCCTCTTCC CCCAGCTGAT GGCCAAGGTA AGCAGGTGCC CTCCAGGGGA ACGAGGTCAC 1020
CTGCTTTGTG CCAGGTGATT GTACTGAATT CGCACCACTG TCCGGGGGCA GGGGCTGCTG 1080
TATCTATTTT ACAGCAGAGG AGGAAACCAA GACATCAGGA GGAGGCCAGC TCGGTTTACA 1140
CAGTTAATGA GAAATGGGCC TATGGCTAGA ACCCAGGAGT GCCTCCCTGC AAAGTCCACA 1200
CTTTCCCCAC CTGGATCTCC AGCTGTCTCC TTGCTGTTAG GGTCACAAGG CAATGCTATG 1260
TGTATCAGAG GCACCTGAGG TTTGCTTTCT GGCTCCACTT TGCCTGGGCC TCAAATGCCC 1320
CTTTTGTGAA GTGGGGCCAG GCTGGTTTGG GGTCCCTGAT AGGCAGGAAC CAGCCCAGGA 1380
CACTTGAGTG CAGTAATGGG GCCTGGGCTT GGATTTGGGA GTAACCACCT GGCCAGCCAA 1440
ACAACGATCT TTTTTTTGAG ACGGAGTTTC ACTCTTGTTG CCCAGGCTGG AGTACAATGG 1500
CGCAATCTCG GCTCACCACA ACCTCTGCCT TCTGGGTTCA ATAGATTTTC CTGCTTCAGC 1560
CTCCTGAATA GCTGGGATTA CAGGCATGCA CCACCACACC CAGCTAATTT TGTATTTTTA 1620
GTAGAGGTGG GGTTTCTCCA TGTTGGTCAG GCTGGTCTCG AACTCCTGAT CTCAGGTGAT 1680
CTGCCCACCT TGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACTG CGCCTGGCCC 1740
TCAAGCATCT CTTGAAGACC TGCCAGGAGG CACTGTGGGG ACACCCAGGG AGGAGCCACA 1800
GTTTCTGTCC TCTGGGAGCT GACACGTGAG CAAGAGTGAG AACACAGGTT TAGGGGCTCC 1860
AGGACTGGGT TTGAATCTTG GGTCTTAGTA GCTGTGTGGT CTTGGGCAGG TGCCTTTGCC 1920
TTGCTCAGCC TTTGGGGCTC CCTCCAAAGA TGGGAATAAC AAGCCTTACT TCAGAGTGCA 1980
TTGTGAGGCT AAAGTGAGAT GGTGTCTGCA AAGCTCCCAG CACGTAGTAG GTGCTCAGTA 2040
AGGTGGTTTC CCCTGCCCAG AACCTCAGAT GACTGTCTTC TAAGTCTGAG AGCAACCAGT 2100
GGGCCTCAAA GGCGATTGAG GGCTGCTTCC CCTGCCCTGC ACCTCCCCCC CGCCCCGTCA 2160
TGCTGGCAGC CCGGGAGCAG TCTCTCACGG TTCTGTGGGC AGCTGGAGAT GGGGCAGAAG 2220
CGGGCGTCAG CTCCACAGTG GGGGCACTGG GAGGTGGGGC CAGGCTTGAC TGGGAGGAGA 2280
GGGAGATGCT GGCTTTTCCT TGGTCCTGCC CCCCGCAGCC TTGCAGTCAG AGGCAGCCCC 2340
AATGAGCCCT CTGCAGTTCT GAGTGCCTTC CTCTCCTGTC TCGCAGAGGG GGAGCCTCAC 2400
AAACCCTGAC AGCAGAAGTG ACTTGCCCAG CGTCGATGGG CGCTGGTGGC AGAGCCAGGC 2460
TGACCCCCAG CCTGAGGCCC ACCCGATCCC GATGCTGCAC TCCTAGCTCC TTGGCGTAGG 2520
TCCCTGGGGC TGTCGGGTGC CCTGGCCTCC CTGGCCTGCC CTGGAGCCAG CTATGAAGGA 2580
ATATTCTGGG GCACATGACT CACAAGGCTG GCCCTTCCAC TTTTTGTTTT CCTTTCTTTT 2640
ACTTTTCCCT AATACGGTCT CCTGTGGCCC TTGCTTCTCC TTTCTTGGGG CTCTGAGATG 2700
GCAGTGCCTT TTGCCCTGGA AAGCCTGTCC TGGCAGAGCT CCTGTTAGCT GTCGACCACA 2760
GCTGCTCAAT CGGGAAGGTT CCAAGGGAGG CCGAGCAAAG GCATCAGAGC TGCACAGACC 2820
TGGGCCATAG CTTGGCTGAC CTACTCCCTA GCTATGTGAC CTTGGACAAG TCGCTTTGCC 2880
TCTCTCAGCC TCAGTTTTCA GATTCAGTTC AATCCAACCA ACATTTATTG AAGACTTGTT 2940
AGTGCCCAGT ATGATATTAG CCATTGCAGG TGGAGCAGCT CCCCTGGGAA CCTCAAGATT 3000
GAGTCGGGGT TGGGTGTAGT GGCTCACACC TGTAATCCCA GCACTTTGGG AGGCTGAAGT 3060
GGGTGCATCA CTTGATCCTA GGACTTGGAG ACCAGCCTGG GCAGCATGAT GAGACCCCGT 3120
CTCTACGAAA AAATACAAAA AATTGGCTGG GCGTGGTGGC GTACACCTGT AGTCCTAGCT 3180
ACTCAGGAGG CTGAAGTGGG AGGATCATTT GAGCCTGGGT AGTAGAGGCT 3230