EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS162-07549 
Organism
Homo sapiens 
Tissue/cell
Plasma_cell_myeloma 
Coordinate
chr3:186130640-186133330 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9853115chr3186131600hg19
TF binding sites/motifs
Number: 28             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr3:186133087-186133105TCTTCCTTCCTTCCTTCC-10.05
EWSR1-FLI1MA0149.1chr3:186133091-186133109CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133095-186133113CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133099-186133117CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133103-186133121CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133107-186133125CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133111-186133129CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133115-186133133CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133119-186133137CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr3:186133127-186133145CCTTCCTTCCCTTGTTTC-6.18
EWSR1-FLI1MA0149.1chr3:186133123-186133141CCTTCCTTCCTTCCCTTG-6.84
EWSR1-FLI1MA0149.1chr3:186133079-186133097CTTTTCTTTCTTCCTTCC-6.98
EWSR1-FLI1MA0149.1chr3:186133083-186133101TCTTTCTTCCTTCCTTCC-8.26
JUN(var.2)MA0489.1chr3:186132576-186132590AAAAGGTGAGTCAT+6.45
MAXMA0058.3chr3:186130978-186130988ACCACGTGCT+6.02
MEF2AMA0052.3chr3:186131764-186131776GCTATTTTTAGT-6.18
MEF2BMA0660.1chr3:186131764-186131776GCTATTTTTAGT-6.62
MEF2CMA0497.1chr3:186131763-186131778GGCTATTTTTAGTTC-6.41
NFYAMA0060.3chr3:186132412-186132423TCTGATTGGCT-6.32
ZNF263MA0528.1chr3:186133083-186133104TCTTTCTTCCTTCCTTCCTTC-6.36
ZNF263MA0528.1chr3:186133091-186133112CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133095-186133116CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133099-186133120CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133103-186133124CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133107-186133128CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133111-186133132CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133115-186133136CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr3:186133087-186133108TCTTCCTTCCTTCCTTCCTTC-7.03
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr3186131140186131200
chr3186131407186132227
Number: 1             
IDChromosomeStartEnd
GH03I186413chr3186131314186133044
Enhancer Sequence
GGCAGGGTTT CACCACACTG GCCGGGCTGG TCTCGAACTC CTGACCTCTG GTGATCCCCC 60
CGCCTTGGCC TCCCAAAGTG CTGGGATTAC AAGCATAAGC CACCGTGCCC AGCCAATACA 120
CTATATTTTA AAATAATGCC ATTTATTGTT TACCCTGTGC CAGGCAAGAG AACAAGTGAT 180
TTAGACACAC AGTCTCATTG CATCCTCACA ATCACCTTAT CAGGAAGGTT CTATCATTAA 240
CCCTGTTTTA AAGATGAAGA AACGTACTCC TAGAGAAGTT GGGTCACCTG CAAGCGGCAT 300
AAGGCAGGCT GTGAACCCAG GTCTGCCTGA TTCCAAAAAC CACGTGCTCT TAACCACTGT 360
ACTCCATTAC CATGTGTGGA GTGCCTACTG GGTGCCAAAA TATAGCATAA GACAGAAGCA 420
GCCAAGGCCA TTCCCGGGGA CCCCAGACCC CAAGGGAAAT GCCTTCCTTC CCCCCAGCCC 480
CTGGAGATGT CCTTGGCTGC CTCCTTCTCA CTGTGCTCTT GACCTTGGCT ACTCTTGGGC 540
AGTACCCAAA AGACCCAGGG AACACACTTC CCCTATTCCA TGTCTCTCAG GACAAATGAG 600
GAATTACAAA TAAACCGTAT TAATTCATCT GTGAACTCCA AGCCTCTGGC ACAGTACCCG 660
GCAATATTTT ACATGGTATA TAGCACCTAA CAGGCTATAT TCAAAAAATA TCAGAAGATA 720
GACGGGAGGA GACGGTCACC ATGCCAGGCA GGGAATGTTT CCAGGGAGAA CTGTAGCTGC 780
AGGGAGTGGG ACTTATCCTG ACTGCCCTGG GAGATCGCTA ATTTAGAGCA CACCAGTGTG 840
ACAGTACATT TCTTTTGAAA TGCAACTCAA AATCCGCTTC CTCCAGGAGG AATGCCAAGT 900
GGCGTCCCGG AACAGGACAA GTTGTACTTC ACAGGAGATG GGAAGCTAGA GGGGGGAAAT 960
GCCATCATTA ATCCACCAAG CAGCAGGGGG TGGGGGCGCT TGCCTCCAAC AGGCATGGCT 1020
GGAAAAATAA GCAGCTCTGG CTTGTGCTCC TCCCTGTGTC CCTGCCACGA CTGTGAAGGG 1080
CTAAGAACAC AGCAGAAAAG GTTCCAGTTC ATTTACAAGC CTCGGCTATT TTTAGTTCAT 1140
CGATCCCTGG GCGCGGTGTG TGTGTGTTGA GGGGGGCCGG GGGACGGGGC TTGCAGAGCT 1200
CACGGTTTGA GGTGGAAGCT GGGGAAAGCT TTAGAATTCT TTTCATAGAA CAGGTACTCT 1260
GTTCACTACG CACCATCCAG CCTCTGGAGA CCTAACCGCT TTTCTTGGGG CAGGAAGAAG 1320
GAGCAGTGTC AGGGGAGGGA GGAGACTGAA ATGAGAAAGG GAACGAGGCA AGAGGCGGTG 1380
ACGCCCTTGT GCCAATGACC AAATTGGGTC AGAAAGAACA ACCTTTTGAA TGCAAGTCAG 1440
GAAATGTGAA TCGCTGCCTC AGCAGGGCCA GGTGCATGCC TAGTGGGTGC CGGCCCAGCC 1500
TGACCAGGGA ACTGTGACTG TACCTCCTGC CGCTCTAGAG AACCAGACCG ATGACCATCT 1560
AGAAGTGCAC TGATCTTTAT TCCTTGCCTG GTGCCCTGTG GCCAGTTCAA TTCCTATTAT 1620
CAACCCCTCC TTAAAGCTGT CAGGGAAAAG GAAGGAGAAG TTCACATTTA AAGATGGATC 1680
TAAATGGTGA AAGAGGTGAA AATCATTGCC TTAAAAGAGA TCACCTGTGG ATTTTGTGAG 1740
TTATTAATTC TATGATCCCT ACCGTGTCTG ATTCTGATTG GCTATATATA AATTAAAAAA 1800
CGGCTCTTTT TTCATATCAC CTCTACAGCC CCTGCAAGTT AAAAATATCA TTACCCGGCT 1860
TTTCTCCTTC TAAGTGTAGG CTGCTTGATT TAAGACATTT TGCAAACTTG TCTTTGTTCC 1920
AAGGATTTTT AAGCAAAAAA GGTGAGTCAT AGTAGCAACT CAATAGATGT TGAGCTGATT 1980
TGTGTTACTA AGAAGTTGTG GGTAAATTGC AGTTTTGAAT TTTTGGAAAC GGAATCATAT 2040
TGTAAATGTC CTGGACAGTT CAACAGTTGT GGGACTCCTC TGGCGAGTCC TATGCAGAAA 2100
CCTCCTCTTA CTTGAGTCAC TCAGCAGCAT TCGATGCAAT CACCCATGGC TTCCTTCTTG 2160
AAACGGGTGT GATTCCTTGA CCCTCACACT CACTTGGCTT GTCCCCAGGT TGCTGACTGT 2220
TCCTTCTCAG GCTCCTCTGC TGTCCTCCCT GCCTCTACCA CACCTCAGTG TACTGGAAGG 2280
ACCTGCATTC TACCTTTGTT CCTCCTGGCT TCATTTCCTC CTTCCTAGAG AAAACTGGAG 2340
GATGCCCATC CTGGCACTCT GATGACTCTC AAATTTCTGC CTGCCTTTTC TTTTCTTTTC 2400
TTTTCTTTTC TTTTCTTTTC TTTTCTTTTC TTTTCTTTTC TTTTCTTTCT TCCTTCCTTC 2460
CTTCCTTCCT TCCTTCCTTC CTTCCTTCCT TCCTTCCCTT GTTTCTTTCT TTCTCTCTCT 2520
CCTTTTTTTT TGTCTTGCTC TATCACTCAG GCTGGAGTGC AGTGTCATGA TCTCAACTCA 2580
CTGCAGCCTC TGCCTCCCGG GTTCAAGCAA TTCTAGTGCC TCAGCCTCCT GAGTAGCTGG 2640
GATTACAGGC GCCAGCCACC ACTCCTGGAT AATTGTTTTG TATTTTTAGT 2690