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

TagContent
EnhancerAtlas ID
HS127-17785 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr2:159979950-159982890 
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:159982097-159982115CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr2:159980430-159980448GCTGCCTTCCTCCCTCCC-6.4
EWSR1-FLI1MA0149.1chr2:159982085-159982103CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr2:159982081-159982099CCTTCCTCCCTCCCTCCC-7.28
EWSR1-FLI1MA0149.1chr2:159982101-159982119CCTTCCTTCCTTCCTTTT-7.95
EWSR1-FLI1MA0149.1chr2:159982089-159982107CCTCCCTCCCTTCCTTCC-8.13
EWSR1-FLI1MA0149.1chr2:159982077-159982095CCTTCCTTCCTCCCTCCC-8.32
EWSR1-FLI1MA0149.1chr2:159982073-159982091CATTCCTTCCTTCCTCCC-8.52
EWSR1-FLI1MA0149.1chr2:159982093-159982111CCTCCCTTCCTTCCTTCC-9.42
ZNF263MA0528.1chr2:159981365-159981386CCCCACCCCCCGCCCTCCTCA-6.13
ZNF263MA0528.1chr2:159982097-159982118CCTTCCTTCCTTCCTTCCTTT-6.16
ZNF263MA0528.1chr2:159982080-159982101TCCTTCCTCCCTCCCTCCCTT-6.46
ZNF263MA0528.1chr2:159982069-159982090TCCCCATTCCTTCCTTCCTCC-6.68
ZNF263MA0528.1chr2:159982093-159982114CCTCCCTTCCTTCCTTCCTTC-6.76
ZNF263MA0528.1chr2:159982076-159982097TCCTTCCTTCCTCCCTCCCTC-6.86
ZNF263MA0528.1chr2:159982089-159982110CCTCCCTCCCTTCCTTCCTTC-7.19
ZNF263MA0528.1chr2:159982085-159982106CCTCCCTCCCTCCCTTCCTTC-7.38
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_02736chr2:159980145-159982215Astrocytes
SE_26759chr2:159980209-159983087Esophagus
SE_38253chr2:159979321-159982881HUVEC
SE_40662chr2:159979342-159983590Left_Ventricle
SE_42049chr2:159980256-159980677LNCaP
SE_42049chr2:159980821-159982113LNCaP
SE_42196chr2:159979444-159983088Lung
SE_45882chr2:159979604-159982204Osteoblasts
SE_45882chr2:159982403-159984140Osteoblasts
SE_48873chr2:159980241-159981376Right_Atrium
SE_55647chr2:159980313-159980679Thymus
SE_55647chr2:159980705-159981947Thymus
SE_65122chr2:159980257-159982207NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2159980842159982052
Number: 1             
IDChromosomeStartEnd
GH02I159122chr2159979455159983023
Enhancer Sequence
ATCAGTGGAA GCTTTCAAGG GACTGGGCTG GGACCCACGC TCCCCTCACC CCACCTCAAC 60
CCCTCCAACA CCTCCCCATA TCTCCCTTCT CACATTCCTC CCCTTACTTC TGAATCTCCT 120
GCCCTGACAG AAATGAAATG GAATTCTGTG GTAGCCACTG TACTGAGTAA ATATTGGAGA 180
AGACATTCCC AAATTACAGG ATTTCTTAGA AGTTACTAAT TTATAGCAAA TGAGTATAAT 240
TTACTTAAAA AGCAGAAATA AACTTTTTCT TATTGAAATA TATATTTGTG CCCCACCTGA 300
GTACATAGCT CTGTGCTAAA CACTGTAAAG AAGCTAAACA GAGACAAAGT TCTCTTCCTC 360
CAACTGCTTT TACTTCGTTT AGGAAATGGA AAGAGTAAAA CCCCCTGCCT CCCACCTCTG 420
TGGTCCCATT CAGTGACGCC AGTCTCCCCT CGTGCCCCCA GCCTCAGGTA CAGCTCAATC 480
GCTGCCTTCC TCCCTCCCGC TGCTGTTTTT CCCAAGTCAT TTAACATCAT ACTGTTTTGT 540
CTTCATACTT GAATTTTGAG CTTTCTTGGG CTGTGGGCAA GGTCTTGCAT AGCTACTCCA 600
GACAGGCCGT GCCAGTGGGT TTCAAACTTG AGTGGGAGGC CAGGTGAGGT GGCTCACACC 660
TATAATCCCA GCACTTTGGG AAGCTGAGGC GGGCGGATCA TTTGAGGTCT GGTGTTCGAG 720
ACCAGCCTGG CCAACATAGT GAAACCCTGT CTCTACTAAA AATACAAAAA TTAGCCGGGT 780
GTGGTGGTGC CTGTCTGTAG GAGGCTGAGG CATAAGAATC ACTTGAACCT GGGAGGCAGA 840
GGTTGCAGTG AGCTGAGATC GCACCACTGC ACTCCATCCT GGGCGACGGA ACGAGATTTT 900
GTCTCAAAAA CAAAAAACAA GCCTGAGTGG GGCATCGGAA TCACTCTGTG GTCTGGGGAG 960
GGGCTGAGAA TTTGCATGTC TAATAAGTTC GCAGGTGATG CTGTTGCTGT TGGTCCAGGG 1020
GCTGGTCTGA ACCCACAGGG AAAGAAAATT CTCAAGGATC CTGCCTTCCT TTTGGAGTCA 1080
GTTACTTCAG GCAGTGGAGG GCTCACTTCC TCCTTGTGCA AACAACAGAA GAGCCCTGTG 1140
GCTTAAGGCC TACTTCCTGA GTTCCTTAGA CAAACTCTGA AATTAGCCAT TCTAGGAAGA 1200
TCGATCTTTC CTCCAGGGAT ATCTTTAAAT CAAAGTTTGT GGTTGTTCAA TTGTTTGTAG 1260
CTATTTTCTT AACCATTCCT ACAAAGCTAA GGAAATCAGC TGCATTTTTT TTTTTTCCAG 1320
AGACAGGGCC TCATTTTATC ACCCAGACTG GAGTACAGTA GCATGAGCAT GACTCACTGC 1380
AGCCTCGACT TGTGTGATCC TCCCGCCTCA GCTCTCCCCA CCCCCCGCCC TCCTCACCAA 1440
GTACAGGCAC GCACCACCAT GCCCAGCTAA TTTTTGTATT TTTTTGTAGA GATGGAGTTT 1500
CACCATGTTT CCCAGGCTGG TCCTGAACTC CTGGGCTCAA GTGATCCTCC CACCTCAGCC 1560
TCACAAAGTG CTGGGATTTC AGGCGTGAGC CACCATGCCC AGCTGGTATT AGATTCTTTA 1620
TGGCACATTG TAATTACTAC CAAAAGTCAG AGGAAGTAAG AGCTAGAGAT TTCCTCCTTG 1680
TGAGCTCACA ACCAGGCATG AATGAAAATA AGGCTTAGGT GGAGTTCTGC CCATACAGAT 1740
TTATTAGTAG GCTGTCACAG CACAGCCACA CAACCTGCTT TATACGCCTG GTGAGGCTCC 1800
AGCTTTGTCC TTTTCAGGAG TCTGCTCTGA CAGCAGCTTG CATTTGGTGT TTACCTGTAG 1860
CACATGAGAC AGTGTTTCAT AGACATTATG TCAGTGTTTT ATTGCTGCCC TGAGAAATTA 1920
CTACAAGCTT ATCTTAAATC TATTATCTCA CAATTCTTTA GGACAGAAGT CCAGGCACAT 1980
CTGGCTCTCT TCTCTAGGTT TCCTTAGGCC AAAATCAAGA CGGTAGCAGG GTGGTGTTCT 2040
GTTAAGGCTC AGGGGATGAA CCACTTCCAG GCTCATTCAG GAGGGCAGAA TTCAGTTCCA 2100
TGTGACTGTA GGACTGAGGT CCCCATTCCT TCCTTCCTCC CTCCCTCCCT TCCTTCCTTC 2160
CTTCCTTTTT TGACAGAGTC TTACTCTGTT GCCCAGGCTG GAGTGCAGTG TCGTGATCTC 2220
GGCTCACTGC AACCTCCGAC TCCCGGGTTC AAGCAATTCT CCTGCCTCAG CCTCCTGAGT 2280
AGCTGGGAAT ACAGGTGCCT ACCACGCCCA GCTAATTTTT TGTATTTTTA GTAGAGATGG 2340
GGTTTCACCA TGTTGGTCAG GCTGGTCTCG AACTCCTGAC CTCAGGTGAT CCACCCGCCT 2400
CGGTCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCTGTTG AGCCCGGCCT AGGTCCCCAT 2460
TTCTTTACTG GCTGTCAGCT GAGGATTCTT CTCAACTTTA GAGGCTGCCT GCATTCCTGT 2520
TTGTGGTTCC CTTCCTTCAT CTTCAATGCC AGAAAGGTGG CTTCCTTCTC ACACTTTAGT 2580
GTCTGACCCT TCCTCCTGCC TTTTCTCACT TCTGCTTTCG AGGGTCTGTG TGATTATAGC 2640
AAGCTTACCC AGATAATCCA GGATAATCTA TTTGAAGGTC ATCTAATTAG TATTCTTAAT 2700
TCCATCTGCA GAGTCCCTAC ATGGTCGTAC CCAGATTGTG TTTGATTCAG TAATGAGGGG 2760
ATGGGATCTT GGAATGATAT CTTTAGAATT TGGCCCACCA AAGGCAGAAT TCAGGTTTTC 2820
CTGCCATTTT ACATCAGGGA CTTAACAATT CCTGGGAATC AGCAGCTGGA CCTGGGGCCA 2880
TTTACTTATC AAACCTAGGG CACCATTCTT AACCTTGAGC CTTACATTTC TGAGGCTTAT 2940