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

TagContent
EnhancerAtlas ID
HS092-01388 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr1:43996760-43999730 
Target genes
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:43998859-43998877CCTCCCTTTCTTCCTTCT-6.52
EWSR1-FLI1MA0149.1chr1:43998851-43998869CCTTCCTTCCTCCCTTTC-8.52
EWSR1-FLI1MA0149.1chr1:43998855-43998873CCTTCCTCCCTTTCTTCC-8.64
EWSR1-FLI1MA0149.1chr1:43998843-43998861AATTCCTTCCTTCCTTCC-8.86
EWSR1-FLI1MA0149.1chr1:43998847-43998865CCTTCCTTCCTTCCTCCC-9.47
RREB1MA0073.1chr1:43996777-43996797CCCCCCACCAGCCCCCTCCG+6.13
RREB1MA0073.1chr1:43998539-43998559ACCCCCTCCACCCCCACACA+6.23
RREB1MA0073.1chr1:43998957-43998977GAGGAGGGGGTGGTTGGGTG-6.39
ZNF263MA0528.1chr1:43998846-43998867TCCTTCCTTCCTTCCTCCCTT-6.28
ZNF263MA0528.1chr1:43998858-43998879TCCTCCCTTTCTTCCTTCTTC-7.16
ZNF263MA0528.1chr1:43998855-43998876CCTTCCTCCCTTTCTTCCTTC-7.63
ZNF740MA0753.2chr1:43997067-43997080CCGCCCCCCCCAC+7.82
ZfxMA0146.2chr1:43997205-43997219CAGGCCGCGCCCCC-6.44
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_00616chr1:43995107-43998898Adipose_Nuclei
SE_00616chr1:43998907-44001249Adipose_Nuclei
SE_04240chr1:43997230-43998647Brain_Anterior_Caudate
SE_05040chr1:43996981-44000130Brain_Cingulate_Gyrus
SE_05962chr1:43995415-44000121Brain_Hippocampus_Middle
SE_07193chr1:43995683-43999544Brain_Hippocampus_Middle_150
SE_08033chr1:43997264-44000544Brain_Inferior_Temporal_Lobe
SE_23218chr1:43996011-43999623Colon_Crypt_1
SE_23829chr1:43996144-43998350Colon_Crypt_2
SE_23829chr1:43999234-43999589Colon_Crypt_2
SE_24870chr1:43996197-43999448Colon_Crypt_3
SE_26649chr1:43995723-44004223Esophagus
SE_27645chr1:43995619-44017587Fetal_Intestine
SE_28595chr1:43995607-44004348Fetal_Intestine_Large
SE_31538chr1:43995971-44000533Gastric
SE_41575chr1:43998407-43998733LNCaP
SE_41575chr1:43998859-44001617LNCaP
SE_47657chr1:43999225-43999586Pancreas
SE_50363chr1:43995694-44004359Sigmoid_Colon
SE_52524chr1:43995689-44000339Small_Intestine
SE_56987chr1:43995814-43998375VACO_400
SE_65452chr1:43996948-43999005Pancreatic_islets
SE_65452chr1:43999008-43999882Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr14399784343998152
chr14399930943999502
Enhancer Sequence
GGTGAGTGAC CCCCCGGCCC CCCACCAGCC CCCTCCGCTC CCGTCCCTTC CCCGCTCTCC 60
TTGCCCTCCC CGCTAGTCCA CCCGGCGGAG CTGGGGGCGG TCCCGGGGGG GACGAGGGCG 120
CCGCTGAGGC CGGGCCGCGC CCCCACCTGC CGCGCCCGCA GCCTCGGCGA AGCCCCCCCT 180
CCACGCCCCA GCCTGGCGGC TCCTCCCCGC TCACCCCGCG GCAGACGCGC CCCCAGCGCT 240
GCTGGCTGGC TCGCTCCCCG CCGCCCCTCG CCGCCTCCCT CCCTCTCCAC CGCACCTTAG 300
CCGCAGCCCG CCCCCCCCAC CCAGCGCAAA GTTTCCCGTT TGCGTTCTTG CTCCCCCTCA 360
TCGGTCCCGC CTCGTCCCCC CTTCTAGCGC GGACGCGCTC CGGGGGCGGC CCTCAGACCC 420
CCCAGCCCCG GGCTCCGGGC GGGTCCAGGC CGCGCCCCCG CCCCCGCCGC ACAGGCGCCC 480
CCTCCCAGCC GGCGGGGGAT CCGCAGCCGG CGCGCCCGGG TCTCGCTCGC GGCCCCGGCG 540
CACGTGCGGT CCCGGGCTGC GCCGGGCGCG AGTTTGAAGC CCCCCCACCC CCTTCGTTCG 600
CGAGCACGGG ATGGGGAGGG GCCGAACGGG CTGTACCCGC CCCCAACCGG GTGCAACGCC 660
CTGGAGGCCC TGGAGCGACC TGTCCCGTGA GGACGTGGCC ACTCGGACCC TCTCCGAAAG 720
TTCACTCAGT GGCCGCCCCG CGTCCCGTCC CGTCCCGTCC CGGCTCCCCA TCGCCGTGCC 780
GGCGTCTCTG TCTCGGCTGC TTTCTGTTTT CCTCGGCGTC TCTGCCTCCC CGTGTCAGTG 840
CCTCCCAATC TCACGCCCCT GCAATCCCAG GGTCTCTCCA GCTGTCTCCA TTCTTTTTCC 900
CCAGGTCACT CTGTTCTTTC TCCCCAGGTC TCTCGATTCT GTCTCCCTGG GTCGTCTTGT 960
TCCCTGTCCC TGAGTCTGTT CTCTCCGCTT GGGTCTCTCT ATTTCCTCTC CCTGGGTCTC 1020
TGTCTCCCTC CTTAAGTCTC TGCCTCTTGT CTCTCACCCA TCTCTTGGTG TCTCTGCACT 1080
CTCTGTGCTA GGCGCCCCCC CATTTCCCTG GAATGCTGCC CCTCTGGTTC TTCCACCCCG 1140
GAGGGGGAGG GGCTAGACTT TCTCCCCATT TCAAGCCCCC CTGCCCCCCA GTGCACGGCC 1200
CCTGAGTTGG AGCAGGTTGG GGGTGGGGAG CGCTACCTGC CTGAGCTGTG AAATGGGAGA 1260
GGGAGGCTGC CCCAGCCTGG GGGTTGTCTG GATCTCCCTG AGGGGCCACA GGGCAGGGCC 1320
GGGAGGCTGG ATTAGGTTGA GGAAGGCTCC ACTTTTGAAG GAACAGGGGC AGGGATCCAG 1380
AGCGATCTGG TGTCGGATCT GGCCTGAGAA GCAGGGAAGT GCACTGGGGT GAGAGGCGTA 1440
GAAAAGGATG TGGGGTGGTG GTTCCAGGCG GGTGCTCATG GGGAGGAATC TGCTGAGAAG 1500
GGAAGATCTG GTGGGGAATC CTTTGGGAGG CTTCGGGGAT CTGAGGGATC CAGAAGAGAG 1560
TTCTGACAGG CTATCTAAGG AAATTTCTGT GCTTAGCTCC TTATTAACTC TTGCTTCAGG 1620
GAGCATGAAA ATCCCTGTTT TTTTACTGAT TATATGAATG AGCCTAGGGC TTCAAGAAGG 1680
AGCAGGTGTA ACTCCCCAAG TACAACCCCC TACATTCTCA GCCCCAGGCA CAGGCCACAC 1740
TTTCTCGTAC CCTCTTGCCT TCATTTCCAC ACTCAGCTCA CCCCCTCCAC CCCCACACAC 1800
ACTCCCTATT CAGCTGCTTT CTTGCCCCCT CTCGCATACC TGGGCCCGCA TGCCGGCCAG 1860
GGCTCAAGAA ATCTGTGCCT GCACACTCTC GCAGCATACC TGTGCACATG CACAGTCATC 1920
CTTGTGTATT TTTGTATATG CACTTTCTTG CACATTTTAC TTGCTCAGTC TCTTATTTGA 1980
AATGTCTTTA TAGTGTTTTT TTTAGTTTCC TTTATAGTTT CCTTTTCCAG CTGCTCTTCC 2040
TCTTCCCTCT TTCTTTCCTT TAACAAGAAA ATTGTTTTAA CATAATTCCT TCCTTCCTTC 2100
CTCCCTTTCT TCCTTCTTCT TGCAACTACT GATACCTCCC CTTTATCCAG CTTTGTGTGC 2160
CCTGGGCGGG TTGGCTTGGT GTACAAGGCT GCCAAGAGAG GAGGGGGTGG TTGGGTGTTG 2220
GTGAAGGAAT TTGGCGGGGC AGAGTTAGAC TGCAGCAAAC GGAAACTAGC TACACATCTT 2280
TTACTGGGAA GTGTATGGAT ACGCAGCAAA ATACTAGCCC TGGCAGTTTG GGCACAGTCC 2340
ACCCTTTTTT CCATCAGCCT GAACTATGGG AGTCTAGCTT TGAGGGTCCT CCCTGGGGGC 2400
GGGGAGGAGG GGACCCAGAC CTCCTGCAGT AGAGGGGTTG TGATACACAC CACGGCTCCT 2460
CCACTTTCCA GCTTCAGGCC TCAAAGAGGC CCCTTTCTCC CTGAGTCTCA ATTTCACTCC 2520
CTGTAAAATG GGGTAGCTAA TCCAACCCGG ACTGGGTCCC AGGGCTGTTG TAAGAATCCA 2580
AGGGAACTGT GTGGCAGTGC ATCGTCAGCA GTGGCAGTCA CTTCCCTTGT GACTGACACT 2640
GCTGTGTGCT TGGTTCCAGC TTGCAGTCAG GGCCCTACCC TCGAGAAGCT CGTGGTCCTT 2700
GGGGGAGCAG GTTGCACCAT GGGATTGCAA AAGCAATTCA GTTACCTGTC ATTGATTGCT 2760
GACTGTGTGC CAGACCCCGG GGTAGGCGCT TTCGGCCCCG GCTGCCTTTC TTCCTTTGGG 2820
ACTAACAGCT ATGTAGAAGA GGCAGCCCAC CCCTAAGGTT CAGGCATCTG CTCAACTAAA 2880
GCAGCTGCGG TTCTGAGTTG GGTTAGAACA TTGCAAGAGT TCATCAAGAG ACGGGGGAGA 2940
GTTCGGAGGT CAGGGTGAGG TGAGTCCCAG 2970