EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS031-21656 
Organism
Homo sapiens 
Tissue/cell
Denditric_cell 
Coordinate
chr7:75245390-75249880 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1186222chr775247329hg19
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr7:75245426-75245437AAAGATAAGAA-6.62
HES2MA0616.2chr7:75247611-75247621GGCACGTGCC+6.02
HES2MA0616.2chr7:75247611-75247621GGCACGTGCC-6.02
IRF1MA0050.2chr7:75247463-75247484TCTTTCTTTCATTTTTTTTCT+6.32
MecomMA0029.1chr7:75245422-75245436AAGAAAAGATAAGA+6.46
Nr2f6(var.2)MA0728.1chr7:75246615-75246630TGAACTCCTGACCTC-6.22
ZNF263MA0528.1chr7:75245935-75245956GGAGGAGGACGAGGAGGAGGA+10.26
ZNF263MA0528.1chr7:75245917-75245938GGAGGAGGAGGAGGAAGAGGA+10.86
ZNF263MA0528.1chr7:75245920-75245941GGAGGAGGAGGAAGAGGAGGA+11.13
ZNF263MA0528.1chr7:75245914-75245935GGAGGAGGAGGAGGAGGAAGA+11.36
ZNF263MA0528.1chr7:75245923-75245944GGAGGAGGAAGAGGAGGAGGA+11.79
ZNF263MA0528.1chr7:75245902-75245923GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr7:75245905-75245926GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr7:75245908-75245929GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr7:75245911-75245932GGAGGAGGAGGAGGAGGAGGA+12.34
ZNF263MA0528.1chr7:75245926-75245947GGAGGAAGAGGAGGAGGACGA+7.25
ZNF263MA0528.1chr7:75245932-75245953AGAGGAGGAGGACGAGGAGGA+8.11
ZNF263MA0528.1chr7:75245899-75245920TGGGGAGGAGGAGGAGGAGGA+8.68
ZNF263MA0528.1chr7:75245938-75245959GGAGGACGAGGAGGAGGAAGA+8.87
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_04465chr7:75246867-75247567Brain_Anterior_Caudate
SE_05143chr7:75246542-75247650Brain_Cingulate_Gyrus
SE_06030chr7:75246418-75249003Brain_Hippocampus_Middle
SE_07279chr7:75246613-75247686Brain_Hippocampus_Middle_150
SE_54400chr7:75245704-75246196Spleen
SE_54400chr7:75246223-75248730Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr77524558975245760
chr77524831075248397
chr77524897175249314
chr77524720075248011
chr77524702475247489
Number: 1             
IDChromosomeStartEnd
GH07I075616chr77524588975248318
Enhancer Sequence
AAGACTCTGT CTCAAAAAAA AAAAAAAAAA AAAAGAAAAG ATAAGAAAAG AAAAGAAAAC 60
AAAAACAAAA ACAAAGTATC TCGTAACATC GTCCTAGACA AGAATGAGAA AGGACAGGCT 120
GCTAGGGGTC CAAACCACCG CCCACCAGCC AAACCTGGCC TCAGCCTGCT TGTGCATGGC 180
CTGTGAGCTA GGACTGGTTT TTGTGTTCTT GTTTAGGGAC AGAGTCTTGC TCTGTTGCCC 240
AGGCTGCAGT GTAGTGGTAC GATCATAGCT CACTACAGCC TTGAACTCCT GGGTTCATGC 300
AATCGTCCCA CCTCCACCTC CCAAGTAGGT GGGCCTACAG GTGCGCACCA CCACGCCAGG 360
CTAATTAAAA AATTTTTTTT TGTAGAGACC GGGTCTCACT TTGTTGCCCA GGCTGGTCTT 420
GAGCTCCTGG CTTCTAGCGA TCCTCCCACC TTAGCCTCCC AAAGTGCTGG AATTACCGGC 480
GCTAGCCACC ATGCCTGGCT TTTTAAGGGT GGGGAGGAGG AGGAGGAGGA GGAGGAGGAG 540
GAAGAGGAGG AGGACGAGGA GGAGGAAGAA ATAGTAGCAG CAGGAAGCCA CAAAGCCAAA 600
AACATTTACC ATCTGGCCCT TTGCAGAAAA TGTTTGCTGG CCCCTGGACT AGGCAGGGCA 660
GCCTATGAGG GTGGATGTCC ACACATACAG AGGCTGATTA CTGGCCATCA CTTTGGGGTA 720
AGGCATGCTG GTGCCTGAGC CTGTGTCCTC CTCCTCATGT TTACCAGGGA GGTATATGTC 780
AGGCACAGTG ATTGATCTAA CTGATGCTGG GAACAACAGT AACTACATTT AGATGACTAT 840
TTTTTTTTGT TTGGACAAGG TCTTGCTCTG TTGCCCAGGT TGGAGTGCAG TGGTGCAATC 900
ATGGCTCATT GCAGCCTCGA CCTCCTGGGC TCAAGCAATC CTCCCACCTC AGCCTCCCAA 960
AATAGTTGGG AGCACAGGTG CATGCCACCA CACCCAGCTA ATTTTTTTTT TTTTTTTTTT 1020
TGAGATGGAG TTTTGCTCTG TCACCTGGCT GGAGTGCAAT GGCGTGATCT CAGCTCACTG 1080
CAACCTCCGC CTCCCCGGCT CAAGCGATTC CCTTGTCTCA GCCTGCCAAG TCGCTGCGAT 1140
TACAGGCACC CACCATCACT CCCGGCTAAT TTGTTTTGTA GTTTTTAGTA GAGACGGGGT 1200
TTCACCATGT TGACCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCT CCTGCCTCGG 1260
CTTCCCAAAG TGCTGGGATT ACAAGCGTGA GCCACCGCAC CCAGCCACTA ATTTTTTATT 1320
ATTTGTAGAG GTGAGGATCT CCCTGTGTTG CCCAGGCTGG TCTCGAACTC CTGGCCTCAA 1380
GCCATCCTCC TGCAGCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGACC CACCGCGCCC 1440
AGCCTCAGCC TGGTTCCTTG CGTGAGTCTT GGTTTCTTGG TCTCCTTTTC CCCGTATGCC 1500
AGCTGCCTCC CTCCATAAGA GAACATCTGT GATGACCTTC GGGGTGCCCA CTTAGGCTTT 1560
CAAAGGGGCC TGGAATGTAG GGCACAGGGT AAGAGACTCG GACACCAGGC CTTGGGGAAA 1620
AGGAGAAGCG GGCCCATATG CCCTCCTCTC ACCCACAGGG AGCTGTGGCT TCGAAAGGGG 1680
CTCCTCCCTT GTAAGGCTGC TGCTCCTGTC GTCATGGAGG AAACCTTGGT TCTGCTTCCC 1740
TAGCACCCCA AACTGCAAAG TCACGCTGGC AGGTATTGCA CCCAGAGGGC TCATTCCCCA 1800
TTCATCATAG TCACTGGTTG GGCAAGTCAC CCTCCCTAGA AAGCGCAGCC TTGGGTAAAT 1860
CCACCAGACA TATCCTGATC TTTCACTATT CACAGAGCCA GACTGGAGTG GCCTTTCGTA 1920
ATGGCCCTGG CCAGAGCTCC CGGGGGAAGC CTTCCGGATA GGCAGCTTGT CAGCAAGAGT 1980
GGGAAACCCT GGGCTGCGCC CTCCCCACAA ACCACCAGCA TTGCCCAACT TCCTCTCTTC 2040
ATGCCCTCTA CCACCCTCTC GTTGCCCCAG CTTTCTTTCT TTCATTTTTT TTCTTGAGAC 2100
ACAGTTTCAC TGTCACCCAG GCTGGAGTGC AGTAGTGTGA TCTCGGCTCA CTGCTACCTA 2160
CCTCCACCTC CTGGGTTCAA GCGATTCTCA CACCTTAGCC TCCCGAGTGG CTGGGATTAC 2220
AGGCACGTGC CACCAACTCT GGCTAATTTT ATATTTTTAG TAGAAACAGG GTTTCACCAT 2280
GTTGGTCAAG CTGGTCTCAA ACTCCTGACC TCAAGTGTTT CATCTGCCTC AGCCTCCCAA 2340
AGTGCTGGGA TTACAGGTGT GAGCTACCAC ACGTGGCTAA TTTTTGTATT TTCAGTAGAG 2400
ATGGGGGTTT CACCATGTTG GCCAGGCTGG TCTTGAACTC CTGACCCCAG GTGACCTGCC 2460
CTCCTCAGTC TCCCAAAGTG CCGGGATTAC AGGCATGAGC CACCGCACCC AGCTGTTTCC 2520
CCAGCTTTCT AACAGTGAGG TTAGTTTTGT CTCTTCTCTT TTATTAATAT ACTGCTACTT 2580
ATCTCCAATG ATCTGAAGAC TCAAGGTGGG TGATGCCTGA CTTACAGGAG ATCCCCCAGC 2640
ACGGGAACCA TCCCTTATCC AGCTCTGGGT CTCTTGCAGT GTCCAATTTC TAGAAGTGAC 2700
CTTTCTGTCA AGTGAATGAG CCAAGCCCCA GCCACATCCC AGCACTAGAA AACCTGATGC 2760
CTCTCCCTTG AGCACATCCT TTTTTTTTTC TTCCAAGTTT TTTTGTAGAG ATGGGGTTTC 2820
ACTATGCTGC CCAGGCTGGT CTCAACCTCC TGGGCTCCAG TGAGCCTCCC ACCTTGGCCT 2880
CCCACCCAAC ATCCTTGACA TCCCACCTTT TGTTCTATTT CTGCAGGAAT CGCTGTGTGT 2940
AGAAAGAAAG CCTTTGGTCA GTGGTTCCCA GACTTGGCTA GGCCGGGATA TCATCTGAGA 3000
ATCCTGTACC CCGAGTTTGT ACACACACCC CTAGATTCCT TTGCTCCACC CCCAAATTGG 3060
ACTCATTTGG GCTCGGAAGG GCCCATGGCA CTGTTAATTC AGGTGATGTT ACAGAAGAAC 3120
ATTGTATGTC AGAGTCTAAG AAAAAATTCA GCTAAAAGTA AAAACAGTGG CCGGGCACAG 3180
TGGCTCATGC CTGTAATCCC AGCACTTTGG GAAGCCCAGG TGGGCGGATC ACTTGAGGTC 3240
AAGAGTTTGA GACCAGCCTG GCCAACATGG TGAAACCCCA TCTCTACTAA AAATACAAAA 3300
ATTAGCCAGG TGTGGTGGCG TGTGCCTGCT GTAATCCCAG CTACTCGGGA GTCTGAGGCA 3360
GGAGGATTGC TTAAACCCAG AAGGCAGAGG TTGCAGTGAG CCGAGATCAC TCCAGCCTGG 3420
GCGACAGAGC AAGACTTTGT CTCAAAAAAA AAAAAAAAAG AGAAGAAAAA CAGTAACAAA 3480
AAGGAAGAAT GAGAGCAAAG AATAAAGATG GTGGAAATGT GAAGAATGAA GTCAGTTTCT 3540
CAGCTCAGAC AAGTATACCT TGATGTAAGT AAATTTTTTT CTGGAAAATG TGAATTGCCA 3600
CTAAGGCCAA ATTAGGAGAT TATTATTCAT TTCACAGAAG ACATTGGCAT TCGATACCCT 3660
TAAATAGCAA TCTCCGTTAG TACATTTAAG AGAGGATTCA GTTTACAGAA GTGTGATTTA 3720
TACAAAACCA CATCTGTTAC ATAAAGCTCA GAAAAATAGC TCTCCTCCCA TGTCATCTTG 3780
CTAACTATAG AACTGGCCCA GTATAGATGG TCACCTATTT TCTTCTAAAA GATACCACCC 3840
CTGCTCTCTG TCATCTATTT CTGTTTCACC GTGATCACGG GTAACAGATT CTTAGGGGCC 3900
ACCCAGATCT CTCTCTGGTC TTCCCTAAAC TCAGGGAACA ACTGCTCTGA ATTGTTTTCA 3960
TATTCACTCA TTCATTCGAC ATATATTTCT GGAAGGCCTA TCATATGCCT GGCACTACTC 4020
TAGAAATACA GTGAGGGTGC GGTGGCTCAT GCCTGTAATC CCAGCGCTTT GGGAGGCCAA 4080
GGTGGGTGGA TTGTTTGAGC CCAGGAGTTC AAGACCAGCT GGGGGCAACA TGGTGAAACC 4140
CTGTCTCTAC AAAAATACAA GAAATTATCC AGGCGTGGTG GTGCATGCTT ATAGTTCCAG 4200
CTACTTGGGA GGCTGAGGTG GGAGGATCAC CTGAGCTCAG GAGGCAGAAG TTGCAGTGAG 4260
CCAATATTGC GCCACTGTAC ACCAGCCTGG GCAACAGAGC AAGACCATGT CTTTAAAAAA 4320
AAAAAAAAAA AAGGCCAGGC ACAATGGCTC ATGCCTGTAA TCCCATCACT TTGGGAGGCC 4380
AAGGTGGGTG GGTCACTTGA GGTCAGAAGT TCGAGACCAG CCTGGCCAAC ATGGTGAAAC 4440
CAGTCTCTAC TGAAAATACA AAAATTAGCC AGGGGTGGTG GTGCATGCCT 4490