EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS139-34122 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr21:34166800-34169240 
Target genes
Number: 2             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2154427chr2134168573hg19
TF binding sites/motifs
Number: 53             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr21:34168345-34168363CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr21:34168349-34168367CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr21:34168353-34168371CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr21:34168257-34168275CATTTCTTCATTTCTTCC-6.08
EWSR1-FLI1MA0149.1chr21:34168229-34168247CATTCATCCCTCCCTTCC-6.22
EWSR1-FLI1MA0149.1chr21:34168297-34168315CCTTCCCTCCTTCCCTCT-6.55
EWSR1-FLI1MA0149.1chr21:34168261-34168279TCTTCATTTCTTCCTTCC-6.79
EWSR1-FLI1MA0149.1chr21:34168265-34168283CATTTCTTCCTTCCTTCT-6.79
EWSR1-FLI1MA0149.1chr21:34168249-34168267CCTTCCTTCATTTCTTCA-6.84
EWSR1-FLI1MA0149.1chr21:34168309-34168327CCCTCTTTCCTTCCCTCC-6.84
EWSR1-FLI1MA0149.1chr21:34168233-34168251CATCCCTCCCTTCCTTCC-7.25
EWSR1-FLI1MA0149.1chr21:34168301-34168319CCCTCCTTCCCTCTTTCC-7.36
EWSR1-FLI1MA0149.1chr21:34168305-34168323CCTTCCCTCTTTCCTTCC-7.69
EWSR1-FLI1MA0149.1chr21:34168289-34168307CCTTCCCTCCTTCCCTCC-7.85
EWSR1-FLI1MA0149.1chr21:34168317-34168335CCTTCCCTCCTTCCCTCC-7.85
EWSR1-FLI1MA0149.1chr21:34168245-34168263CCTTCCTTCCTTCATTTC-7.97
EWSR1-FLI1MA0149.1chr21:34168329-34168347CCCTCCTTCCTTCCCTCC-8.34
EWSR1-FLI1MA0149.1chr21:34168269-34168287TCTTCCTTCCTTCTTTCC-8.52
EWSR1-FLI1MA0149.1chr21:34168293-34168311CCCTCCTTCCCTCCTTCC-8.7
EWSR1-FLI1MA0149.1chr21:34168321-34168339CCCTCCTTCCCTCCTTCC-8.7
EWSR1-FLI1MA0149.1chr21:34168281-34168299CTTTCCTTCCTTCCCTCC-8.84
EWSR1-FLI1MA0149.1chr21:34168313-34168331CTTTCCTTCCCTCCTTCC-9.05
EWSR1-FLI1MA0149.1chr21:34168241-34168259CCTTCCTTCCTTCCTTCA-9.09
EWSR1-FLI1MA0149.1chr21:34168277-34168295CCTTCTTTCCTTCCTTCC-9.09
EWSR1-FLI1MA0149.1chr21:34168325-34168343CCTTCCCTCCTTCCTTCC-9.09
EWSR1-FLI1MA0149.1chr21:34168337-34168355CCTTCCCTCCTTCCTTCC-9.09
EWSR1-FLI1MA0149.1chr21:34168357-34168375CCTTCCTTCCTTCCTTCA-9.09
EWSR1-FLI1MA0149.1chr21:34168273-34168291CCTTCCTTCTTTCCTTCC-9.17
EWSR1-FLI1MA0149.1chr21:34168237-34168255CCTCCCTTCCTTCCTTCC-9.42
EWSR1-FLI1MA0149.1chr21:34168341-34168359CCCTCCTTCCTTCCTTCC-9.72
EWSR1-FLI1MA0149.1chr21:34168285-34168303CCTTCCTTCCCTCCTTCC-9.93
EWSR1-FLI1MA0149.1chr21:34168333-34168351CCTTCCTTCCCTCCTTCC-9.93
ZNF263MA0528.1chr21:34168269-34168290TCTTCCTTCCTTCTTTCCTTC-6.02
ZNF263MA0528.1chr21:34168313-34168334CTTTCCTTCCCTCCTTCCCTC-6.35
ZNF263MA0528.1chr21:34168337-34168358CCTTCCCTCCTTCCTTCCTTC-6.67
ZNF263MA0528.1chr21:34168237-34168258CCTCCCTTCCTTCCTTCCTTC-6.76
ZNF263MA0528.1chr21:34168301-34168322CCCTCCTTCCCTCTTTCCTTC-6.76
ZNF263MA0528.1chr21:34168285-34168306CCTTCCTTCCCTCCTTCCCTC-6.8
ZNF263MA0528.1chr21:34168273-34168294CCTTCCTTCTTTCCTTCCTTC-6.93
ZNF263MA0528.1chr21:34168345-34168366CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr21:34168349-34168370CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr21:34168353-34168374CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr21:34168325-34168346CCTTCCCTCCTTCCTTCCCTC-6
ZNF263MA0528.1chr21:34168574-34168595GGAGGAGGCGAGAGGAGGGGG+7.06
ZNF263MA0528.1chr21:34168293-34168314CCCTCCTTCCCTCCTTCCCTC-7.1
ZNF263MA0528.1chr21:34168341-34168362CCCTCCTTCCTTCCTTCCTTC-7.24
ZNF263MA0528.1chr21:34168281-34168302CTTTCCTTCCTTCCCTCCTTC-7.56
ZNF263MA0528.1chr21:34168333-34168354CCTTCCTTCCCTCCTTCCTTC-7.58
ZNF263MA0528.1chr21:34168289-34168310CCTTCCCTCCTTCCCTCCTTC-7.79
ZNF263MA0528.1chr21:34168317-34168338CCTTCCCTCCTTCCCTCCTTC-7.79
ZNF263MA0528.1chr21:34168309-34168330CCCTCTTTCCTTCCCTCCTTC-7.87
ZNF263MA0528.1chr21:34168321-34168342CCCTCCTTCCCTCCTTCCTTC-7.92
ZNF263MA0528.1chr21:34168329-34168350CCCTCCTTCCTTCCCTCCTTC-8.5
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr213416692934167422
chr213416853934168823
Number: 1             
IDChromosomeStartEnd
GH21I032794chr213416712134167270
Enhancer Sequence
AAGAAAAGAG GCAGCTTTAT CACAACCTTT CATTTGAAAT ACACAGCTTA TGGAAAAGGA 60
ACCCCAGAAA AAAACAAGTT GTAAACATTT CTTTCTTGCA GTTCTAGTAA CTGTTTCCTG 120
AGCCACAGGC AATGCTTGCA GCCCAGGCAC TGGCAAGCTC TTTTCTCAGC ACCTCATCCA 180
GAGACAGCAG CCAAACCTTT GAGCTCTGCT CATCTGAGGT GTAAAACTCC CAGTGATGTT 240
GGCTGACAGT GAGACCAACA TGCCAACAAC ACAGCCAGAG CGATGCCAGA GCGGATGCCA 300
GAGAGGAGAC CTACCGCATC CTATCTATGG GCAGGGATTT GGAGTTGAAA GAGCACATTC 360
TCCAAACATC CAATTACTAG CATGAAGCGC CCAAAAACCC CTGAACATGA CATGCTTTCC 420
TCCCCCTCAA TATCTGACTT CCTGGAATTC GGGAGACAAA CACTTCTTTG TTGGATTCAG 480
CTATCCAAGC GCTACCTATT ACACAACATA GCATGAATAC CAATGAAGCA TTTAGTTAAT 540
GGCAAGCTTT AATTTCTAAG TAGATAAACA TGCCTCCCAT CCCCACCATA TTAATCTGTT 600
TGTGAGTCCA TTCATCCTGT TCAGGGCCTC TTACAAATGT ACCTAGGTAA CTGTGGTAAT 660
AGACAACAAA AAGACTAATC ACCCACCGAT TAATCACAAT TATTTTGACT TAGCTACTCT 720
TATGCCAGAA GAAATTTATG AACTGATCTT GTCAATGTAT TGCAGGGCTC CAAAACAAAA 780
CCATATATAA GAACTTCTAA AAAATCTAAA TAAGGTAGGG ATGCATGGGT AATTTAAAGA 840
GCAGCACCAA TGTCCAGTTT TGGGTAAAAG CCCTACAGTG TCTGGCATAT GACAGATGCA 900
GGATCCTCCT TTGTGGTGTG ATTGGAATGA GATGAGATGA GCATTATGGC AGAGTGTACC 960
ACATTTCAGT TTGGCGAAAG TAATAACATT CCCCCAATGA CTGAGGAGAG AAACCAAACA 1020
ATACAATTCA GTCTTCTCCA TTTGCTAAGC TCCATGGGTG TGGTGGGATA CTTGGCATGC 1080
GACCTCTGAG TGGGAGGGCC CAGAGCTACT GGCAGGGCCA CTACACTAAG GGCCAGGGAG 1140
CCACAGATGG AAGGGTCAGT CTGAAGAGCT CAACATGTGT CCAAAGAGTA CAGTGACAGC 1200
AGGAAAGAGG CTAGGCAGAC AAGCAGCAAT TAGGGTGTAA GATGAGGCCA CAAGGCAATT 1260
AGAAATCCAA AGGAATCAAG GCTAAAAATG CCAGGGATCG GGTAGACAGG CAGGAGGCAC 1320
AAGCCACAAC CCCATGGCTG GGATGCCAGG AGGATAGAAG TAAGCTCTGC CGCGTAAACT 1380
TGAACAGAGG GTGAGACATT GATTCACAGC AACTGTGACT GTATTCATGC ATTCATCCCT 1440
CCCTTCCTTC CTTCCTTCAT TTCTTCATTT CTTCCTTCCT TCTTTCCTTC CTTCCCTCCT 1500
TCCCTCCTTC CCTCTTTCCT TCCCTCCTTC CCTCCTTCCT TCCCTCCTTC CTTCCTTCCT 1560
TCCTTCCTTC CTTCAACTAA TGCTTATTGG AAGATTACTA GGTGGCATGC CCTCTGCTAG 1620
CCATGGGGGT ACAACTCAGA ACAAGACAAC CCAGGGCCCA GTCCTCATAG AACTTATGTC 1680
CTAACGAAAT TGATTCTGCT TCCAATGGGC TGGGGCGTCA TAGCCCAAAG CCAGGCCCGT 1740
CCTGCATGTG AGGATGGAGA GGCTATAGCA GTGGGGAGGA GGCGAGAGGA GGGGGCAAAT 1800
GCAGGAGTTA GGCAGGGCCC AGCCTGGGCT GTGTGCCAGG CCCTGGCTTA GGCCAAGCAG 1860
AAGAAACAAA GATACAAAAG ACCTGGATCC TATCCTCCAG GATTTATCCT CAAAGGAAAA 1920
AGACCAATAA GGCTGAACTG AGAAGCACTG TACTGAACAT ACAGGCGGCT ATGAGAACAT 1980
AGCAGAGAGA GAGAGAGATT CGACGCGGGG GACTGGATAA GGCGGTTTAG AGTGCTTTGT 2040
ATCTATTTTG AAGTTGGCAC AGGATTTTCT TAAAGGCTTC TTATTAAATG TATTAATAGG 2100
TACATTTTGT CATGAAAGAA AGAGCTTTGA GAAACGTGGA GAACAAGCGT TCTCCCTGAA 2160
CAAGAGGCTT AACAGTCTTA AGCAGTGTTA GAATGTGGGT GTGTCTACCC CCTTAGTGAG 2220
GAACGGTGTA TAATTTATTA ATTACAAGAT AATTTTAGAC AATCAGCTGT CCCAGATTCC 2280
ACTGGAGGCC TCTGGGACTT CGTGTCCCAG TAACCCTGTT ATCCCAGAAC CAGGAATGCT 2340
GTCAATACTG TTGGCCCACC CTGACCCTAG CCTTAAAAGA AAAAAGAGGG GAGAGGTCTA 2400
TTCATCAGCC CGAACCTAGT GAGAAAAGTG TCTGCCTCCC 2440