EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-22157 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr9:130975760-130979800 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2502731chr9130976557hg19
TF binding sites/motifs
Number: 32             
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
EWSR1-FLI1MA0149.1chr9:130975786-130975804GGAAAGAAAGTAGGAAGG+6.6
EWSR1-FLI1MA0149.1chr9:130975765-130975783GGAAGGGAGGGAGGGAGG+7.08
FOXP1MA0481.2chr9:130978377-130978389ATCTGTTTACTT-6.74
FOXP2MA0593.1chr9:130978378-130978389TCTGTTTACTT-6.32
GATA2MA0036.3chr9:130975808-130975819GAAGATAAGAA-6.02
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
ZNF263MA0528.1chr9:130975771-130975792GAGGGAGGGAGGGTGGGAAAG+6.03
ZNF263MA0528.1chr9:130975762-130975783GATGGAAGGGAGGGAGGGAGG+6.25
ZNF263MA0528.1chr9:130975775-130975796GAGGGAGGGTGGGAAAGAAAG+6.27
ZNF263MA0528.1chr9:130976338-130976359CCCCCCTTGCCTTCCACCTCC-6.38
ZNF263MA0528.1chr9:130975767-130975788AAGGGAGGGAGGGAGGGTGGG+6
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: 5             
ChromosomeStartEnd
chr9130976556130978716
chr9130979056130979435
chr9130976600130977800
chr9130976017130976107
chr9130978792130978931
Number: 1             
IDChromosomeStartEnd
GH09I128214chr9130976758130979266
Enhancer Sequence
TTGATGGAAG GGAGGGAGGG AGGGTGGGAA AGAAAGTAGG AAGGATGAGA AGATAAGAAA 60
TAAGGGAAGG TAATAGGCTC TGCTTAATAG GGAGAAAGAT TGCTGTGGAG AGAGCACCTA 120
CCCGGACTCA GGAGCCCTAC CTTGTCACCA ACTTGCACCA TGATCTTGGG CAAGACTCTT 180
CCCTTTTGTG CCTCAGTTTC TACCCTATAC AATGAAGCCG ATGGTAGAGC TCATCTTCCA 240
TTCCCTCTTT TGGTCAGTGC GGGTGTCCTG AGAGTCTGCT ACATGCCAGA CCCAGGGCTA 300
GGTGCTGGGA TATTGTGACA AACAAGTCTA GCCTAGTCCC TGCTCCCGGG GCCATCAGAA 360
CATCAAGGAA AGCCAAGGCC AGAACTGCCC TGCAGTGTTC AGACCTCAGC TTGAAATTCA 420
TGAGCTGTGA CGGGGCTGCC TAGGGTCCCC TGGGGCAGCA GGAACAGAGA GCGACTTGTT 480
GCCTGGGGGT AGCCTCACCT CCTCCCAACT GTATTTCTTG GCCTACCCAC TCCCTTGCAG 540
GCACCCCAAC TCCCTGCTTC AGAGCACGCC CCTGCCCACC CCCCTTGCCT TCCACCTCCA 600
GGGTCAAGAT CTGGCTGGAA ATATCCTGCC CTCACCCCCA AGCTCACTGC CATCCTCCAG 660
GAAACCCACC GTCCAACTCT CTCCCCGCTG CCTCTTCTGG TGACGAGGCT GTGGGAGTCC 720
AGCCTGTGGT CTCAGCATGC CCAGCAAGCT ATCGTTATTT ATAATCATAG TAGCCACGAT 780
TGGTTCAGCC ATCAGTCTGT ATAAGCCTCA CAGCAACCCA TTTTACTGAT GTGGAAACTG 840
AGGCTCAGAG AGGTATGGTC ATTTGTGCAC AGCCACACAG CTCCTACATG ACAGCTCAGA 900
CATTCAATGT GGGGTCCATC TGACATCAGA GCCCAAAAAA GAGGAGGCAT AGAAGAATGA 960
CCGGCACTGG GTGCACGCCC AGTTAAGCAC GTTACTTCCT GGGGTCATTT GCATTCAGCA 1020
GGGCCTGGGA ACCAGGATCC CAGAGCTCTG ATCCCAAGTC TCAGGTCCTA GAGTAGGGGT 1080
AGGGGTAGGG GTCACATCAG CCCTTGGGTT CAGTTTCTCC AGACCCCTCT CACGGTGACA 1140
ACTCCAGTTC AGACAGGGAG TGTGGCATTT GGGGTTCCTG AGAGGTGTTT GTTTCGTCCC 1200
CTCATGTTTC ACGTTTGAAG GTGCCTCTGC AGATGGCCAG GCACAGCCTC CCTGGGAACC 1260
CACCATCTGC TCCAAATGAG TGGGGAGAAC TGGCATGCCA GCAGCCGCCC CTCCCACGCT 1320
GGGCACAGCA CGCGGCCTCC GAGGCTGGTG GGCCTGATAC TTTTCTCTGG GCACCTGTTC 1380
TGTCCTCCCT TAGCCTAACC AGGAGCTGGA GGCTGGATCT AGTCTGGATC CCCACTGGGG 1440
AGAAGGAGGG CCACCTAGGG GACCCTTAAA CAGAGGGCTA AAGTGGGACA GTGTGTCCAG 1500
GTGAAAGGGA AGAGCTAGGG AGCTGCTGAG TCATGCACAT TCCTTCTCGT GTTGCCTGCA 1560
CGCCTACTAC GTGCGGGGCC TGTGCCAGGC AGGAACCCGG AAGTGAGTGA GGAGCTCATT 1620
GTCCGGACCT GGGGACCTGC TGGTCCTCCC CACTGTCAGT CCAGACGTGA GACTGGGAAG 1680
CAGACCTCTC GGGTCCTGGC ACCAGGCACC AGGCCAAGGA AAGGCCAATG TAGGATTCGA 1740
TGAAGGAGCC AGCCTGGCAC TGGCTCCTCA GCATGGGGCA GATGGTCCTT AAACTTAACA 1800
CGGAGTGTGG AAACCACCTG AGGATCCATT TAAAACCCAG ATTCTGCCTC CCCATGAAGC 1860
CCTCTTGAGA TTCTAGCCCA GCATGCCTGA GGAGCATGCG TCTGGACAAA CTACCCAAGG 1920
CATTCTGATG CAGGCCGCGT GAGGGCCTCA CTTTGAGAAC CTGGGCCATG ACAGAGATGG 1980
GCCACCTCCC CATCTGGGCA CCAGGAGATC TTGGCTCTGG GAGGGGTTGA CCCCCAGACA 2040
TGGCCCTGCC TCTAGTCTCT GCTTCCCAGA AGCTACTTGC CCTTTAAGTA GCCCTGGGGA 2100
GGCAGCAGGC AGCTGGCCCA GACCCTGACC ACCCAGCATT CTTGCCAGCT GGGCCCTGGG 2160
CTCCCCACAC CCGCTATGTG GCACCTTGGA GACCTCCACC CCTCAGGCTC ACCAGGGCTG 2220
CGTGGGCCTG TCTGCTCAAG GAGAGGCCTC TCAGGGAAGA ACTCCAGGGA AAGTCCACGT 2280
CTCTGTGTGG GGGACTCTTT GTGGGGAGTC CCATCCTTTC CAGCCCCTCC TGCAGTTTCC 2340
ATGGCAACTA CTGTTGCCAT GGTGTTGCTG GTGAGGAGCT GGTGGAGAAG AGGGTGGACC 2400
CCCGGCCCCC ACACCCACCC CAGCTTCTAT GAGAACAGCT GTTCTATCTC CACAGCCCTG 2460
GGGGACTCCC AAAACTGGAA GTCACGCCCC CAAAGGAGTC TTTGAGTAAA GGATGGGAGA 2520
GATTGAGACC GGAAGTCCTC CCACCCCCCA GCAAACCCCC TCCCTCTGTG CCGCCTGGCA 2580
CACCTCTGTT CTAGCACATA CCACGCTGCA TTGCATTATC TGTTTACTTG TCTGTCTCTC 2640
CCACCACACT GTGAGTTCCT CAGGGTGGGA ACTGTCTGAC TCATCATCTC CCATCCCCAG 2700
AGCCCGGCAC AGGGCCCGGC ACAGACTGAA TTTAATTGAA TTACATAAAA AGCCAAGTCT 2760
GGCTTCTTGG GTTTGAGACA GCACCATTGA ATGAGGAAGT TTCCAGGCTG AGGGTCCAAC 2820
AGACACTCAG CTTTGAATCC CCACTCTGCT GTGTGACCTT GGGTGAGTCA CTTCACCTCT 2880
CTGAGCCTCA GCTGCTTCCT CTGTAAAATG ATAATCTCTA TATCAGAGCA CAGATTCGAG 2940
GACTTGGAGA TTCAATCAGA ATTTATTGAG TGCCCCTTGT GTGCTAAGCC CTGTCCTGGG 3000
CACTGGGATA CAGTGGCAGA CAGAAAGAGG CTGCCCTGCT CACTGTCTGG CAAGAATGAA 3060
AAGCATTTGC CTGGTGCGCA GAAATGATGA ATATACACAG GGCTTACCAT CCTTCTCCTT 3120
CTCCAGTATA ATTCCTGACT CCTCCCCAGC AGCGTCCACT TCCCCAGACG TGAGGCAGTG 3180
GAGAGGCTTC AAGAGGGGGC TTTGAACCTA GGAGCTCTGG GTCTAGTCTG TTGTACCTAA 3240
GACCCTTAGC TCCTGACCCT GGGGTGCAAG AAGACTTGTG AGTCTGGGTC AGGCTCTGGG 3300
CTGGGAGCAA GAGACCTGGG TTCCACCTCT GGCTCTGTAG AGCTTGAATG TATCTTTTTC 3360
CCTCCCTGGG CCTCTCCATG AATAAGGCGC TGGCTGTGTC TCAATGGTCC CTCGGGCTTC 3420
AACCTGTTCC CCCCTTTCCT GGGCCCTGGA GATCCCATGA CTGGCAATTC TGACATCCTG 3480
ATTCCTGGAG AGGCCTTCAC CCTTGTGCTT GCGCCAGCTG GAGGGTGGTG CAGAGGGAGG 3540
TGGATGAAAA GAGCTGACTG GACAGAGAAC CGGCACCCAC AAGAGTCAGC CAAAAGGACA 3600
GCTGAGGTTG ACATTGGCAC GAGCAGATGT CTAAGCTATA GACTGTCAGG TCTGGGGACG 3660
GGGGATGACT TTGGGACCTC TCAGTCCAGT CCTTCAAAGG CGGCTCGGTT CACAGGGGGC 3720
TGAAGGGCAG GGGAGTGTCA CTGCAGAGTC AAATATATCC GAGACCAGGG TCTGCTCTGC 3780
CAGATACTGG CTGTGCAACC TGAATGTCTC TAAGGTGCAG CTCCCTCATC TGCAAAATGG 3840
GGGTAATAAC AGCACCTGCC TCATGGGGCT ACAGTATGGA GCCCCACTAA GCGCCTGGCA 3900
TGCAGTAGGC ACTAAGAAGC ATGAGTTTTT TTGTTTCTTT GTGGGTTTTT TTGAGGTGGA 3960
GTTTTGCTCT TGTCGCCTAG GCTGGAGTGC AATGGCGCGA TCTTGGCTCA CCGTAACCTC 4020
CGCCTCCCGG GTTCAAACAA 4040