EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-39606 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr9:130976490-130979740 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2502731chr9130976557hg19
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EHFMA0598.2chr9:130977353-130977365AACCCGGAAGTG+6.74
ELF1MA0473.2chr9:130977353-130977365AACCCGGAAGTG+7.22
ELF3MA0640.1chr9:130977353-130977366AACCCGGAAGTGA+7.22
ELF4MA0641.1chr9:130977353-130977365AACCCGGAAGTG+7.22
ELF5MA0136.2chr9:130977354-130977365ACCCGGAAGTG+6.32
FOXP1MA0481.2chr9:130978377-130978389ATCTGTTTACTT-6.74
FOXP2MA0593.1chr9:130978378-130978389TCTGTTTACTT-6.32
GLIS3MA0737.1chr9:130978056-130978070CTTTGTGGGGAGTC-6.16
MSCMA0665.1chr9:130978193-130978203AACAGCTGTT+6.02
MSCMA0665.1chr9:130978193-130978203AACAGCTGTT-6.02
MYF6MA0667.1chr9:130978193-130978203AACAGCTGTT+6.02
MYF6MA0667.1chr9:130978193-130978203AACAGCTGTT-6.02
NFE2L1MA0089.2chr9:130977281-130977296GCTGCTGAGTCATGC-6.64
Nfe2l2MA0150.2chr9:130977283-130977298TGCTGAGTCATGCAC-6.66
PHOX2AMA0713.1chr9:130978492-130978503TAATTGAATTA-6.14
Phox2bMA0681.1chr9:130978492-130978503TAATTGAATTA-6.14
RFX1MA0509.2chr9:130978093-130978109AGTTTCCATGGCAACT-6.33
RFX1MA0509.2chr9:130978093-130978109AGTTTCCATGGCAACT+6.35
RFX2MA0600.2chr9:130978093-130978109AGTTTCCATGGCAACT+6.67
RFX2MA0600.2chr9:130978093-130978109AGTTTCCATGGCAACT-6.72
RFX5MA0510.2chr9:130978093-130978109AGTTTCCATGGCAACT-6.61
RFX5MA0510.2chr9:130978093-130978109AGTTTCCATGGCAACT+6.6
STAT3MA0144.2chr9:130977821-130977832CTTCCCAGAAG-6.14
ZBTB7AMA0750.2chr9:130977354-130977367ACCCGGAAGTGAG+6.15
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_65793chr9:130976260-130978472Pancreatic_islets
SE_65793chr9:130978750-130979599Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9130976556130978716
chr9130979056130979435
chr9130976600130977800
chr9130978792130978931
Number: 1             
IDChromosomeStartEnd
GH09I128214chr9130976758130979266
Enhancer Sequence
CTCAGCATGC CCAGCAAGCT ATCGTTATTT ATAATCATAG TAGCCACGAT TGGTTCAGCC 60
ATCAGTCTGT ATAAGCCTCA CAGCAACCCA TTTTACTGAT GTGGAAACTG AGGCTCAGAG 120
AGGTATGGTC ATTTGTGCAC AGCCACACAG CTCCTACATG ACAGCTCAGA CATTCAATGT 180
GGGGTCCATC TGACATCAGA GCCCAAAAAA GAGGAGGCAT AGAAGAATGA CCGGCACTGG 240
GTGCACGCCC AGTTAAGCAC GTTACTTCCT GGGGTCATTT GCATTCAGCA GGGCCTGGGA 300
ACCAGGATCC CAGAGCTCTG ATCCCAAGTC TCAGGTCCTA GAGTAGGGGT AGGGGTAGGG 360
GTCACATCAG CCCTTGGGTT CAGTTTCTCC AGACCCCTCT CACGGTGACA ACTCCAGTTC 420
AGACAGGGAG TGTGGCATTT GGGGTTCCTG AGAGGTGTTT GTTTCGTCCC CTCATGTTTC 480
ACGTTTGAAG GTGCCTCTGC AGATGGCCAG GCACAGCCTC CCTGGGAACC CACCATCTGC 540
TCCAAATGAG TGGGGAGAAC TGGCATGCCA GCAGCCGCCC CTCCCACGCT GGGCACAGCA 600
CGCGGCCTCC GAGGCTGGTG GGCCTGATAC TTTTCTCTGG GCACCTGTTC TGTCCTCCCT 660
TAGCCTAACC AGGAGCTGGA GGCTGGATCT AGTCTGGATC CCCACTGGGG AGAAGGAGGG 720
CCACCTAGGG GACCCTTAAA CAGAGGGCTA AAGTGGGACA GTGTGTCCAG GTGAAAGGGA 780
AGAGCTAGGG AGCTGCTGAG TCATGCACAT TCCTTCTCGT GTTGCCTGCA CGCCTACTAC 840
GTGCGGGGCC TGTGCCAGGC AGGAACCCGG AAGTGAGTGA GGAGCTCATT GTCCGGACCT 900
GGGGACCTGC TGGTCCTCCC CACTGTCAGT CCAGACGTGA GACTGGGAAG CAGACCTCTC 960
GGGTCCTGGC ACCAGGCACC AGGCCAAGGA AAGGCCAATG TAGGATTCGA TGAAGGAGCC 1020
AGCCTGGCAC TGGCTCCTCA GCATGGGGCA GATGGTCCTT AAACTTAACA CGGAGTGTGG 1080
AAACCACCTG AGGATCCATT TAAAACCCAG ATTCTGCCTC CCCATGAAGC CCTCTTGAGA 1140
TTCTAGCCCA GCATGCCTGA GGAGCATGCG TCTGGACAAA CTACCCAAGG CATTCTGATG 1200
CAGGCCGCGT GAGGGCCTCA CTTTGAGAAC CTGGGCCATG ACAGAGATGG GCCACCTCCC 1260
CATCTGGGCA CCAGGAGATC TTGGCTCTGG GAGGGGTTGA CCCCCAGACA TGGCCCTGCC 1320
TCTAGTCTCT GCTTCCCAGA AGCTACTTGC CCTTTAAGTA GCCCTGGGGA GGCAGCAGGC 1380
AGCTGGCCCA GACCCTGACC ACCCAGCATT CTTGCCAGCT GGGCCCTGGG CTCCCCACAC 1440
CCGCTATGTG GCACCTTGGA GACCTCCACC CCTCAGGCTC ACCAGGGCTG CGTGGGCCTG 1500
TCTGCTCAAG GAGAGGCCTC TCAGGGAAGA ACTCCAGGGA AAGTCCACGT CTCTGTGTGG 1560
GGGACTCTTT GTGGGGAGTC CCATCCTTTC CAGCCCCTCC TGCAGTTTCC ATGGCAACTA 1620
CTGTTGCCAT GGTGTTGCTG GTGAGGAGCT GGTGGAGAAG AGGGTGGACC CCCGGCCCCC 1680
ACACCCACCC CAGCTTCTAT GAGAACAGCT GTTCTATCTC CACAGCCCTG GGGGACTCCC 1740
AAAACTGGAA GTCACGCCCC CAAAGGAGTC TTTGAGTAAA GGATGGGAGA GATTGAGACC 1800
GGAAGTCCTC CCACCCCCCA GCAAACCCCC TCCCTCTGTG CCGCCTGGCA CACCTCTGTT 1860
CTAGCACATA CCACGCTGCA TTGCATTATC TGTTTACTTG TCTGTCTCTC CCACCACACT 1920
GTGAGTTCCT CAGGGTGGGA ACTGTCTGAC TCATCATCTC CCATCCCCAG AGCCCGGCAC 1980
AGGGCCCGGC ACAGACTGAA TTTAATTGAA TTACATAAAA AGCCAAGTCT GGCTTCTTGG 2040
GTTTGAGACA GCACCATTGA ATGAGGAAGT TTCCAGGCTG AGGGTCCAAC AGACACTCAG 2100
CTTTGAATCC CCACTCTGCT GTGTGACCTT GGGTGAGTCA CTTCACCTCT CTGAGCCTCA 2160
GCTGCTTCCT CTGTAAAATG ATAATCTCTA TATCAGAGCA CAGATTCGAG GACTTGGAGA 2220
TTCAATCAGA ATTTATTGAG TGCCCCTTGT GTGCTAAGCC CTGTCCTGGG CACTGGGATA 2280
CAGTGGCAGA CAGAAAGAGG CTGCCCTGCT CACTGTCTGG CAAGAATGAA AAGCATTTGC 2340
CTGGTGCGCA GAAATGATGA ATATACACAG GGCTTACCAT CCTTCTCCTT CTCCAGTATA 2400
ATTCCTGACT CCTCCCCAGC AGCGTCCACT TCCCCAGACG TGAGGCAGTG GAGAGGCTTC 2460
AAGAGGGGGC TTTGAACCTA GGAGCTCTGG GTCTAGTCTG TTGTACCTAA GACCCTTAGC 2520
TCCTGACCCT GGGGTGCAAG AAGACTTGTG AGTCTGGGTC AGGCTCTGGG CTGGGAGCAA 2580
GAGACCTGGG TTCCACCTCT GGCTCTGTAG AGCTTGAATG TATCTTTTTC CCTCCCTGGG 2640
CCTCTCCATG AATAAGGCGC TGGCTGTGTC TCAATGGTCC CTCGGGCTTC AACCTGTTCC 2700
CCCCTTTCCT GGGCCCTGGA GATCCCATGA CTGGCAATTC TGACATCCTG ATTCCTGGAG 2760
AGGCCTTCAC CCTTGTGCTT GCGCCAGCTG GAGGGTGGTG CAGAGGGAGG TGGATGAAAA 2820
GAGCTGACTG GACAGAGAAC CGGCACCCAC AAGAGTCAGC CAAAAGGACA GCTGAGGTTG 2880
ACATTGGCAC GAGCAGATGT CTAAGCTATA GACTGTCAGG TCTGGGGACG GGGGATGACT 2940
TTGGGACCTC TCAGTCCAGT CCTTCAAAGG CGGCTCGGTT CACAGGGGGC TGAAGGGCAG 3000
GGGAGTGTCA CTGCAGAGTC AAATATATCC GAGACCAGGG TCTGCTCTGC CAGATACTGG 3060
CTGTGCAACC TGAATGTCTC TAAGGTGCAG CTCCCTCATC TGCAAAATGG GGGTAATAAC 3120
AGCACCTGCC TCATGGGGCT ACAGTATGGA GCCCCACTAA GCGCCTGGCA TGCAGTAGGC 3180
ACTAAGAAGC ATGAGTTTTT TTGTTTCTTT GTGGGTTTTT TTGAGGTGGA GTTTTGCTCT 3240
TGTCGCCTAG 3250