EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS159-04457 
Organism
Homo sapiens 
Tissue/cell
Pancreatic_islet 
Coordinate
chr3:186130990-186133910 
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-FLI1MA0149.1chr3:186133833-186133851CCCTGCTTCCTCCCTTGC-6.08
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
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
TAACCACTGT ACTCCATTAC CATGTGTGGA GTGCCTACTG GGTGCCAAAA TATAGCATAA 60
GACAGAAGCA GCCAAGGCCA TTCCCGGGGA CCCCAGACCC CAAGGGAAAT GCCTTCCTTC 120
CCCCCAGCCC CTGGAGATGT CCTTGGCTGC CTCCTTCTCA CTGTGCTCTT GACCTTGGCT 180
ACTCTTGGGC AGTACCCAAA AGACCCAGGG AACACACTTC CCCTATTCCA TGTCTCTCAG 240
GACAAATGAG GAATTACAAA TAAACCGTAT TAATTCATCT GTGAACTCCA AGCCTCTGGC 300
ACAGTACCCG GCAATATTTT ACATGGTATA TAGCACCTAA CAGGCTATAT TCAAAAAATA 360
TCAGAAGATA GACGGGAGGA GACGGTCACC ATGCCAGGCA GGGAATGTTT CCAGGGAGAA 420
CTGTAGCTGC AGGGAGTGGG ACTTATCCTG ACTGCCCTGG GAGATCGCTA ATTTAGAGCA 480
CACCAGTGTG ACAGTACATT TCTTTTGAAA TGCAACTCAA AATCCGCTTC CTCCAGGAGG 540
AATGCCAAGT GGCGTCCCGG AACAGGACAA GTTGTACTTC ACAGGAGATG GGAAGCTAGA 600
GGGGGGAAAT GCCATCATTA ATCCACCAAG CAGCAGGGGG TGGGGGCGCT TGCCTCCAAC 660
AGGCATGGCT GGAAAAATAA GCAGCTCTGG CTTGTGCTCC TCCCTGTGTC CCTGCCACGA 720
CTGTGAAGGG CTAAGAACAC AGCAGAAAAG GTTCCAGTTC ATTTACAAGC CTCGGCTATT 780
TTTAGTTCAT CGATCCCTGG GCGCGGTGTG TGTGTGTTGA GGGGGGCCGG GGGACGGGGC 840
TTGCAGAGCT CACGGTTTGA GGTGGAAGCT GGGGAAAGCT TTAGAATTCT TTTCATAGAA 900
CAGGTACTCT GTTCACTACG CACCATCCAG CCTCTGGAGA CCTAACCGCT TTTCTTGGGG 960
CAGGAAGAAG GAGCAGTGTC AGGGGAGGGA GGAGACTGAA ATGAGAAAGG GAACGAGGCA 1020
AGAGGCGGTG ACGCCCTTGT GCCAATGACC AAATTGGGTC AGAAAGAACA ACCTTTTGAA 1080
TGCAAGTCAG GAAATGTGAA TCGCTGCCTC AGCAGGGCCA GGTGCATGCC TAGTGGGTGC 1140
CGGCCCAGCC TGACCAGGGA ACTGTGACTG TACCTCCTGC CGCTCTAGAG AACCAGACCG 1200
ATGACCATCT AGAAGTGCAC TGATCTTTAT TCCTTGCCTG GTGCCCTGTG GCCAGTTCAA 1260
TTCCTATTAT CAACCCCTCC TTAAAGCTGT CAGGGAAAAG GAAGGAGAAG TTCACATTTA 1320
AAGATGGATC TAAATGGTGA AAGAGGTGAA AATCATTGCC TTAAAAGAGA TCACCTGTGG 1380
ATTTTGTGAG TTATTAATTC TATGATCCCT ACCGTGTCTG ATTCTGATTG GCTATATATA 1440
AATTAAAAAA CGGCTCTTTT TTCATATCAC CTCTACAGCC CCTGCAAGTT AAAAATATCA 1500
TTACCCGGCT TTTCTCCTTC TAAGTGTAGG CTGCTTGATT TAAGACATTT TGCAAACTTG 1560
TCTTTGTTCC AAGGATTTTT AAGCAAAAAA GGTGAGTCAT AGTAGCAACT CAATAGATGT 1620
TGAGCTGATT TGTGTTACTA AGAAGTTGTG GGTAAATTGC AGTTTTGAAT TTTTGGAAAC 1680
GGAATCATAT TGTAAATGTC CTGGACAGTT CAACAGTTGT GGGACTCCTC TGGCGAGTCC 1740
TATGCAGAAA CCTCCTCTTA CTTGAGTCAC TCAGCAGCAT TCGATGCAAT CACCCATGGC 1800
TTCCTTCTTG AAACGGGTGT GATTCCTTGA CCCTCACACT CACTTGGCTT GTCCCCAGGT 1860
TGCTGACTGT TCCTTCTCAG GCTCCTCTGC TGTCCTCCCT GCCTCTACCA CACCTCAGTG 1920
TACTGGAAGG ACCTGCATTC TACCTTTGTT CCTCCTGGCT TCATTTCCTC CTTCCTAGAG 1980
AAAACTGGAG GATGCCCATC CTGGCACTCT GATGACTCTC AAATTTCTGC CTGCCTTTTC 2040
TTTTCTTTTC TTTTCTTTTC TTTTCTTTTC TTTTCTTTTC TTTTCTTTTC TTTTCTTTCT 2100
TCCTTCCTTC CTTCCTTCCT TCCTTCCTTC CTTCCTTCCT TCCTTCCCTT GTTTCTTTCT 2160
TTCTCTCTCT CCTTTTTTTT TGTCTTGCTC TATCACTCAG GCTGGAGTGC AGTGTCATGA 2220
TCTCAACTCA CTGCAGCCTC TGCCTCCCGG GTTCAAGCAA TTCTAGTGCC TCAGCCTCCT 2280
GAGTAGCTGG GATTACAGGC GCCAGCCACC ACTCCTGGAT AATTGTTTTG TATTTTTAGT 2340
AGAGATGGGG TTTCACTATG TTGGCCAGCC TTGTCTTAAA CCTCTGACCT CAGGTGATCT 2400
GCCCACCTCG GCCTCCCAAA GTGCTGGGAT TAGAGGCTTG AGCCACCGCA CCTGGTCGAC 2460
TGCCAAATTT CTATCTCTAG CTGGATCTCT CGCTGAGTTC TAGATGTGCA AACACCACTG 2520
CCTGCTGGCC ATCATCACCT GCCTGTCCGT TAGGCAGCTC GAACTTAGCA AGGACAAAAT 2580
TGATAGATTG CTTTTTATCC CTTAAAATAT ACCTCTCCCC TAGTGTTCCC CATTTCAGTA 2640
TATGTGGCAT CATCAACCCA GCTGCTAGAG CCAAAAAACC AGCAATCATT CTTGATTCCT 2700
CTCTTTCGTT CATCCCCTAC ACTCAATTCA TTTGTAATCC TGCTGGTTCT AATGCAGTGT 2760
ATAATCAGGA TCTGGTCACT TCTCAGCACC TCTGCTGTTC TGCCATCCCT CCCTGGACTA 2820
TTTCACCAGC CTCTTTCCCA GGTCCCTGCT TCCTCCCTTG CCTTCCAGTC CATCCTCCAT 2880
AGAACAGAGC AATCCTTTTA AAAATATAAA TCAGACTCTA 2920