EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-45956 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr2:159980260-159983550 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs34324915chr2159983207hg19
TF binding sites/motifs
Number: 18             
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
LHX2MA0700.1chr2:159983018-159983028ACTAATTAAC+6.02
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: 2             
IDChromosomeStartEnd
GH02I159122chr2159979455159983023
GH02I159126chr2159983261159983410
Enhancer Sequence
CTGTGCTAAA CACTGTAAAG AAGCTAAACA GAGACAAAGT TCTCTTCCTC CAACTGCTTT 60
TACTTCGTTT AGGAAATGGA AAGAGTAAAA CCCCCTGCCT CCCACCTCTG TGGTCCCATT 120
CAGTGACGCC AGTCTCCCCT CGTGCCCCCA GCCTCAGGTA CAGCTCAATC GCTGCCTTCC 180
TCCCTCCCGC TGCTGTTTTT CCCAAGTCAT TTAACATCAT ACTGTTTTGT CTTCATACTT 240
GAATTTTGAG CTTTCTTGGG CTGTGGGCAA GGTCTTGCAT AGCTACTCCA GACAGGCCGT 300
GCCAGTGGGT TTCAAACTTG AGTGGGAGGC CAGGTGAGGT GGCTCACACC TATAATCCCA 360
GCACTTTGGG AAGCTGAGGC GGGCGGATCA TTTGAGGTCT GGTGTTCGAG ACCAGCCTGG 420
CCAACATAGT GAAACCCTGT CTCTACTAAA AATACAAAAA TTAGCCGGGT GTGGTGGTGC 480
CTGTCTGTAG GAGGCTGAGG CATAAGAATC ACTTGAACCT GGGAGGCAGA GGTTGCAGTG 540
AGCTGAGATC GCACCACTGC ACTCCATCCT GGGCGACGGA ACGAGATTTT GTCTCAAAAA 600
CAAAAAACAA GCCTGAGTGG GGCATCGGAA TCACTCTGTG GTCTGGGGAG GGGCTGAGAA 660
TTTGCATGTC TAATAAGTTC GCAGGTGATG CTGTTGCTGT TGGTCCAGGG GCTGGTCTGA 720
ACCCACAGGG AAAGAAAATT CTCAAGGATC CTGCCTTCCT TTTGGAGTCA GTTACTTCAG 780
GCAGTGGAGG GCTCACTTCC TCCTTGTGCA AACAACAGAA GAGCCCTGTG GCTTAAGGCC 840
TACTTCCTGA GTTCCTTAGA CAAACTCTGA AATTAGCCAT TCTAGGAAGA TCGATCTTTC 900
CTCCAGGGAT ATCTTTAAAT CAAAGTTTGT GGTTGTTCAA TTGTTTGTAG CTATTTTCTT 960
AACCATTCCT ACAAAGCTAA GGAAATCAGC TGCATTTTTT TTTTTTCCAG AGACAGGGCC 1020
TCATTTTATC ACCCAGACTG GAGTACAGTA GCATGAGCAT GACTCACTGC AGCCTCGACT 1080
TGTGTGATCC TCCCGCCTCA GCTCTCCCCA CCCCCCGCCC TCCTCACCAA GTACAGGCAC 1140
GCACCACCAT GCCCAGCTAA TTTTTGTATT TTTTTGTAGA GATGGAGTTT CACCATGTTT 1200
CCCAGGCTGG TCCTGAACTC CTGGGCTCAA GTGATCCTCC CACCTCAGCC TCACAAAGTG 1260
CTGGGATTTC AGGCGTGAGC CACCATGCCC AGCTGGTATT AGATTCTTTA TGGCACATTG 1320
TAATTACTAC CAAAAGTCAG AGGAAGTAAG AGCTAGAGAT TTCCTCCTTG TGAGCTCACA 1380
ACCAGGCATG AATGAAAATA AGGCTTAGGT GGAGTTCTGC CCATACAGAT TTATTAGTAG 1440
GCTGTCACAG CACAGCCACA CAACCTGCTT TATACGCCTG GTGAGGCTCC AGCTTTGTCC 1500
TTTTCAGGAG TCTGCTCTGA CAGCAGCTTG CATTTGGTGT TTACCTGTAG CACATGAGAC 1560
AGTGTTTCAT AGACATTATG TCAGTGTTTT ATTGCTGCCC TGAGAAATTA CTACAAGCTT 1620
ATCTTAAATC TATTATCTCA CAATTCTTTA GGACAGAAGT CCAGGCACAT CTGGCTCTCT 1680
TCTCTAGGTT TCCTTAGGCC AAAATCAAGA CGGTAGCAGG GTGGTGTTCT GTTAAGGCTC 1740
AGGGGATGAA CCACTTCCAG GCTCATTCAG GAGGGCAGAA TTCAGTTCCA TGTGACTGTA 1800
GGACTGAGGT CCCCATTCCT TCCTTCCTCC CTCCCTCCCT TCCTTCCTTC CTTCCTTTTT 1860
TGACAGAGTC TTACTCTGTT GCCCAGGCTG GAGTGCAGTG TCGTGATCTC GGCTCACTGC 1920
AACCTCCGAC TCCCGGGTTC AAGCAATTCT CCTGCCTCAG CCTCCTGAGT AGCTGGGAAT 1980
ACAGGTGCCT ACCACGCCCA GCTAATTTTT TGTATTTTTA GTAGAGATGG GGTTTCACCA 2040
TGTTGGTCAG GCTGGTCTCG AACTCCTGAC CTCAGGTGAT CCACCCGCCT CGGTCTCCCA 2100
AAGTGCTGGG ATTACAGGCG TGAGCTGTTG AGCCCGGCCT AGGTCCCCAT TTCTTTACTG 2160
GCTGTCAGCT GAGGATTCTT CTCAACTTTA GAGGCTGCCT GCATTCCTGT TTGTGGTTCC 2220
CTTCCTTCAT CTTCAATGCC AGAAAGGTGG CTTCCTTCTC ACACTTTAGT GTCTGACCCT 2280
TCCTCCTGCC TTTTCTCACT TCTGCTTTCG AGGGTCTGTG TGATTATAGC AAGCTTACCC 2340
AGATAATCCA GGATAATCTA TTTGAAGGTC ATCTAATTAG TATTCTTAAT TCCATCTGCA 2400
GAGTCCCTAC ATGGTCGTAC CCAGATTGTG TTTGATTCAG TAATGAGGGG ATGGGATCTT 2460
GGAATGATAT CTTTAGAATT TGGCCCACCA AAGGCAGAAT TCAGGTTTTC CTGCCATTTT 2520
ACATCAGGGA CTTAACAATT CCTGGGAATC AGCAGCTGGA CCTGGGGCCA TTTACTTATC 2580
AAACCTAGGG CACCATTCTT AACCTTGAGC CTTACATTTC TGAGGCTTAT TACAATCTGG 2640
CCTGCTAGAT TTTTATATTT GGGTCACACA CAGGCAGAGT GTTTCTGACA TTTCCAGTCA 2700
ACTCCCTTAC CTCAAATATC ATCAATTTCA CCACTGAAAA TGTTCCAACA GCTGTAATAC 2760
TAATTAACAA AGTCAGTAAT TTAACCAATA TGAAAGCCCA TTTCTGACCC AAAGTATACT 2820
AGTTAACATA ACCTGCTCTT GGTTGGTGAT AAGGATAGCT AGCAGACTGG CTTGCAGTAG 2880
TGTCTCTTGA GTGTGGCTTT TTGATTAAAA GCTGGTTAAC TACTCTTGGA GCCTGTCTTC 2940
CAGATTAAGA CAATTCATTG CTTTTAGGCA GTTGGCTTAC AGCCACTGGA CATATCCCAG 3000
CTTATGTTGA AGTGTTTTGA AATAAAATTC AAATGATATA GTAGACTCTT GCCATCTTAA 3060
CCGAGAGCAT CGAGAGTTCA GTCATGTCTG TGGTTCTCAC CCTTGTGCCT GGTATGCAGT 3120
GGATGTGTCA CAGATATTTG TTGAGTAAAT AAAATGAATT AATGCATTTC CATGCTTTCA 3180
TATATAACAA TTTTAGTACA GTGTGAGAAC AGCATGACAG ATTGCACTGG AAGAAAGCAG 3240
AAATGTTACT CAAGTTACTT TGTTGTACTA GGAGCTTATT GTACTCATGA 3290