EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS068-04766 
Organism
Homo sapiens 
Tissue/cell
GM18526 
Coordinate
chr6:26340980-26343370 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs9467715chr626341301hg19
rs4711107chr626342749hg19
rs9379850chr626343057hg19
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Lhx3MA0135.1chr6:26341591-26341604AAATTAATTAATA+6.37
NKX2-5MA0063.2chr6:26343061-26343071CTCAAGTGGT-6.02
POU6F1MA0628.1chr6:26341593-26341603ATTAATTAAT+6.02
POU6F1MA0628.1chr6:26341593-26341603ATTAATTAAT-6.02
ZNF263MA0528.1chr6:26342309-26342330GAAGGAGGAGAAGAGTGGAGT+6.05
ZNF263MA0528.1chr6:26342175-26342196AGAGAAGGAGGGAGGGAGAGG+6.18
ZNF263MA0528.1chr6:26342283-26342304GAGGGAGAGGAGAGAGGGAGG+6.23
ZNF263MA0528.1chr6:26342299-26342320GGAGGAACGGGAAGGAGGAGA+6.23
ZNF263MA0528.1chr6:26342152-26342173GAAGGAGGGATGGAGAGGAAG+6.24
ZNF263MA0528.1chr6:26342267-26342288AGGTGAGGAGTGGGAGGAGGG+6.24
ZNF263MA0528.1chr6:26342359-26342380AAAGGAGCAGGGGAGGAGGGA+6.29
ZNF263MA0528.1chr6:26342139-26342160AGAGGAAGAGAGAGAAGGAGG+6.32
ZNF263MA0528.1chr6:26342165-26342186AGAGGAAGAGAGAGAAGGAGG+6.32
ZNF263MA0528.1chr6:26342130-26342151GAGGGATGGAGAGGAAGAGAG+6.54
ZNF263MA0528.1chr6:26342156-26342177GAGGGATGGAGAGGAAGAGAG+6.54
ZNF263MA0528.1chr6:26342182-26342203GAGGGAGGGAGAGGAAGAGAT+6.59
ZNF263MA0528.1chr6:26342296-26342317GAGGGAGGAACGGGAAGGAGG+6.65
ZNF263MA0528.1chr6:26342340-26342361GAAGGAGGAATGAGAGGTGAA+6.68
ZNF263MA0528.1chr6:26342362-26342383GGAGCAGGGGAGGAGGGAAAG+6.82
ZNF263MA0528.1chr6:26342270-26342291TGAGGAGTGGGAGGAGGGAGA+7.06
ZNF263MA0528.1chr6:26342178-26342199GAAGGAGGGAGGGAGAGGAAG+7.17
ZNF263MA0528.1chr6:26342279-26342300GGAGGAGGGAGAGGAGAGAGG+8.91
ZfxMA0146.2chr6:26341819-26341833CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_43581chr6:26339710-26344501MM1S
SE_66505chr6:26342011-26342675Jurkat
SE_67190chr6:26339710-26344501MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr62634165526343252
Number: 1             
IDChromosomeStartEnd
GH06I026341chr62634162926343207
Enhancer Sequence
TTTCCTATAG AAACAATGGC ATATTTCAGC AACTACCATA TGCTGATCAC TGTTTAGGAA 60
TGCAAAAAAT ATATCATTCT TGTAGAAGAT GTTTATTTTC AGTCTTTAAA TGAAATCTCT 120
CTTAATAGCA GGCTCAATTC AAAATCATCT TCTAGTTTTT AAAAATTCGT AGATACGTGG 180
ACTTTTGGAA CATGTTTTCT AAAAGGACCC CAACCACCTT TTTATGGATT CAGTTTTGTG 240
TCCCCCAAAA TTCATATGTT GAAATCCTAA TCCTAGTACC TCAGAATGTA ACCTTATTTG 300
GATATAGCTT TGGGAGGACC TGAGGCAGAG CTGTAGGGTG TAGGGGAAGC TGTGGATGCT 360
TCCTGGTTCC TCTGGGTGTG AATGTGGCTG ACGGGTTCAG AGGCTGAGGA TACCTCGCCA 420
GGATGCTGAG GAAAGAAGCC AGGATTTTAG TGGTTCTGCA CTCAGAAACC AGGGCACAAG 480
AACGCAGAGG CAGATGCCCT AGTGGACAGA CGACCAGGGA GGGCCAGCGG TTCTTCTCCA 540
TGCGTGGACA CAGGAGCGGT CTTCTCTTCA TGTCCAAACT GAGATACCAT CTGAGGAAAA 600
GGAGAGGCCC AAAATTAATT AATAAAGCCC TGAATTGACT AGGACGAAGA CCATTATTGA 660
CTCAGGAGTA GCCTGGTTTG ACTAAGATGA AGGATATGCC ATTAAGCGGG AAGGGGCAGA 720
GGATGGAAAT AAAGCTCAGT TTGCATTCAT ATAAACGTAC AGGCGCGCAC CATCATGCCC 780
GGCTAATTTT TGTGTTTTTA TTGGTCAGGC TGATCTCGAA CTCCTGAGCT CGCGATCAGC 840
CCGCCTCGGC CTCCCAAAGT GTTGGGATTA CAGGCGTGAG CCACCACGCC TGGCAACGCC 900
TCTAGGAGCA AAACGTGCAT TTCAGCTTTT GAGGTTCCCT GCTGTGCACA GCCCTCAGCT 960
TGCCATCTAT AGGCCGCTCC ATTGACAGGG GTTGAGAGGG TGAGACTTTC TCAGGCCCAC 1020
GGCACAGGCA GTGATGCATA TCCGCCATGA GGGGGCGGCG AAGCCTAGAG AAAGAGAGAG 1080
ACACCTGAGA CGAGTTCGAA GAGGCGGGAG GAGGGAAAAA GCTGGGGCGG GAGGAAAGGG 1140
GACGGGCAGG GAGGGATGGA GAGGAAGAGA GAGAAGGAGG GATGGAGAGG AAGAGAGAGA 1200
AGGAGGGAGG GAGAGGAAGA GATGATAGAG TGAGGGAACG AGGAGGAGAC GAGGAGGACT 1260
TGTGGGAGGA AAGAGAGAGC AGAGAAAAGG TGAGGAGTGG GAGGAGGGAG AGGAGAGAGG 1320
GAGGAACGGG AAGGAGGAGA AGAGTGGAGT ACGAGGGAAA GAAGGAGGAA TGAGAGGTGA 1380
AAGGAGCAGG GGAGGAGGGA AAGCAAGTTA CTGAAGGGGA AAAACAGTTC TCTGGACAGC 1440
AGTTAGCGAC AGTTGTAGAG TACTTTACAT TTTACAGTGT GTCACAGATA CTGGCTCATG 1500
TTTCCCTCAC AGTAACAACC CAATTAAGCG GTAAGCAGTA ATTGCTGTCC ACGTATTATT 1560
TTCAACCTGA AATGTTATTT TTAACAAAAC ATACTTTATA TATGACAAAA TAAAGAGAAA 1620
CATTGGGGCA AGTGTACAGA CTAATGAACA TTTACTACGT TTTAGTTTAG TGGTTTTTTG 1680
TTTTGTTTTG GTTTGGTTTT GACACAGAGT TTCACTCCTG TCACCCAGGC TGAAGTGCAA 1740
TGGTGCTGTC TTGGCTCACT GTAACCTCTG CCTCCCCAGT TCAAGCGATT CTCGTGCCTC 1800
AGCCTCCTAA GTAGCTGGGA TTGCAAGCAT GCGTCACCAT GCCTGGCTAA TTTTTTATAT 1860
TTTTAGTAAA GACAGGGTTT CACCATGTTG GCCAAGTTGG TCTTGAACTC CTGGCCTCAA 1920
GTGATCCAGC CACCTCGGTC CCTCAAAGTG CTGGGATTAC AGGCATGAGC CACCAAGCCC 1980
GGCCTTGTTT TTTGAGACAG AGTCTCAAAA ACCAAGGCTC TGTTGCCCAG GCTGGAATGC 2040
GGTGACACAA TCACAGCTCA CTGCAGCTCC AACCTCCCGG GCTCAAGTGG TTCCTCCCAC 2100
CTCAGCCTCT ATAGTAGCTG GGACTACAGG CATGAGCCAC CATGTGTGAG CTACATTTCA 2160
TGGTCTCTTT AAATCCATTT CTATGTTAAT TCTCAGATCT CTGAATAGCA TGTCACCAAA 2220
AAGCATGCTG TCTGAGCATG TCAGAGCTCA GACACAGAGG CAAAGGGACA GAGCAGCACA 2280
CAAAACTTAA CAGAAGTGCG TTCTCAAGGA GTCGGCTTGC TAATGGTACA GAGAGAAAAT 2340
AAGTAACACG TAATGTCAGA TGATGACTTA AATGTTATGG AGAAAAATTA 2390