EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-83498 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr9:130976570-130979550 
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: 3             
ChromosomeStartEnd
chr9130979056130979435
chr9130976600130977800
chr9130978792130978931
Number: 1             
IDChromosomeStartEnd
GH09I128214chr9130976758130979266
Enhancer Sequence
CAGCAACCCA TTTTACTGAT GTGGAAACTG AGGCTCAGAG AGGTATGGTC ATTTGTGCAC 60
AGCCACACAG CTCCTACATG ACAGCTCAGA CATTCAATGT GGGGTCCATC TGACATCAGA 120
GCCCAAAAAA GAGGAGGCAT AGAAGAATGA CCGGCACTGG GTGCACGCCC AGTTAAGCAC 180
GTTACTTCCT GGGGTCATTT GCATTCAGCA GGGCCTGGGA ACCAGGATCC CAGAGCTCTG 240
ATCCCAAGTC TCAGGTCCTA GAGTAGGGGT AGGGGTAGGG GTCACATCAG CCCTTGGGTT 300
CAGTTTCTCC AGACCCCTCT CACGGTGACA ACTCCAGTTC AGACAGGGAG TGTGGCATTT 360
GGGGTTCCTG AGAGGTGTTT GTTTCGTCCC CTCATGTTTC ACGTTTGAAG GTGCCTCTGC 420
AGATGGCCAG GCACAGCCTC CCTGGGAACC CACCATCTGC TCCAAATGAG TGGGGAGAAC 480
TGGCATGCCA GCAGCCGCCC CTCCCACGCT GGGCACAGCA CGCGGCCTCC GAGGCTGGTG 540
GGCCTGATAC TTTTCTCTGG GCACCTGTTC TGTCCTCCCT TAGCCTAACC AGGAGCTGGA 600
GGCTGGATCT AGTCTGGATC CCCACTGGGG AGAAGGAGGG CCACCTAGGG GACCCTTAAA 660
CAGAGGGCTA AAGTGGGACA GTGTGTCCAG GTGAAAGGGA AGAGCTAGGG AGCTGCTGAG 720
TCATGCACAT TCCTTCTCGT GTTGCCTGCA CGCCTACTAC GTGCGGGGCC TGTGCCAGGC 780
AGGAACCCGG AAGTGAGTGA GGAGCTCATT GTCCGGACCT GGGGACCTGC TGGTCCTCCC 840
CACTGTCAGT CCAGACGTGA GACTGGGAAG CAGACCTCTC GGGTCCTGGC ACCAGGCACC 900
AGGCCAAGGA AAGGCCAATG TAGGATTCGA TGAAGGAGCC AGCCTGGCAC TGGCTCCTCA 960
GCATGGGGCA GATGGTCCTT AAACTTAACA CGGAGTGTGG AAACCACCTG AGGATCCATT 1020
TAAAACCCAG ATTCTGCCTC CCCATGAAGC CCTCTTGAGA TTCTAGCCCA GCATGCCTGA 1080
GGAGCATGCG TCTGGACAAA CTACCCAAGG CATTCTGATG CAGGCCGCGT GAGGGCCTCA 1140
CTTTGAGAAC CTGGGCCATG ACAGAGATGG GCCACCTCCC CATCTGGGCA CCAGGAGATC 1200
TTGGCTCTGG GAGGGGTTGA CCCCCAGACA TGGCCCTGCC TCTAGTCTCT GCTTCCCAGA 1260
AGCTACTTGC CCTTTAAGTA GCCCTGGGGA GGCAGCAGGC AGCTGGCCCA GACCCTGACC 1320
ACCCAGCATT CTTGCCAGCT GGGCCCTGGG CTCCCCACAC CCGCTATGTG GCACCTTGGA 1380
GACCTCCACC CCTCAGGCTC ACCAGGGCTG CGTGGGCCTG TCTGCTCAAG GAGAGGCCTC 1440
TCAGGGAAGA ACTCCAGGGA AAGTCCACGT CTCTGTGTGG GGGACTCTTT GTGGGGAGTC 1500
CCATCCTTTC CAGCCCCTCC TGCAGTTTCC ATGGCAACTA CTGTTGCCAT GGTGTTGCTG 1560
GTGAGGAGCT GGTGGAGAAG AGGGTGGACC CCCGGCCCCC ACACCCACCC CAGCTTCTAT 1620
GAGAACAGCT GTTCTATCTC CACAGCCCTG GGGGACTCCC AAAACTGGAA GTCACGCCCC 1680
CAAAGGAGTC TTTGAGTAAA GGATGGGAGA GATTGAGACC GGAAGTCCTC CCACCCCCCA 1740
GCAAACCCCC TCCCTCTGTG CCGCCTGGCA CACCTCTGTT CTAGCACATA CCACGCTGCA 1800
TTGCATTATC TGTTTACTTG TCTGTCTCTC CCACCACACT GTGAGTTCCT CAGGGTGGGA 1860
ACTGTCTGAC TCATCATCTC CCATCCCCAG AGCCCGGCAC AGGGCCCGGC ACAGACTGAA 1920
TTTAATTGAA TTACATAAAA AGCCAAGTCT GGCTTCTTGG GTTTGAGACA GCACCATTGA 1980
ATGAGGAAGT TTCCAGGCTG AGGGTCCAAC AGACACTCAG CTTTGAATCC CCACTCTGCT 2040
GTGTGACCTT GGGTGAGTCA CTTCACCTCT CTGAGCCTCA GCTGCTTCCT CTGTAAAATG 2100
ATAATCTCTA TATCAGAGCA CAGATTCGAG GACTTGGAGA TTCAATCAGA ATTTATTGAG 2160
TGCCCCTTGT GTGCTAAGCC CTGTCCTGGG CACTGGGATA CAGTGGCAGA CAGAAAGAGG 2220
CTGCCCTGCT CACTGTCTGG CAAGAATGAA AAGCATTTGC CTGGTGCGCA GAAATGATGA 2280
ATATACACAG GGCTTACCAT CCTTCTCCTT CTCCAGTATA ATTCCTGACT CCTCCCCAGC 2340
AGCGTCCACT TCCCCAGACG TGAGGCAGTG GAGAGGCTTC AAGAGGGGGC TTTGAACCTA 2400
GGAGCTCTGG GTCTAGTCTG TTGTACCTAA GACCCTTAGC TCCTGACCCT GGGGTGCAAG 2460
AAGACTTGTG AGTCTGGGTC AGGCTCTGGG CTGGGAGCAA GAGACCTGGG TTCCACCTCT 2520
GGCTCTGTAG AGCTTGAATG TATCTTTTTC CCTCCCTGGG CCTCTCCATG AATAAGGCGC 2580
TGGCTGTGTC TCAATGGTCC CTCGGGCTTC AACCTGTTCC CCCCTTTCCT GGGCCCTGGA 2640
GATCCCATGA CTGGCAATTC TGACATCCTG ATTCCTGGAG AGGCCTTCAC CCTTGTGCTT 2700
GCGCCAGCTG GAGGGTGGTG CAGAGGGAGG TGGATGAAAA GAGCTGACTG GACAGAGAAC 2760
CGGCACCCAC AAGAGTCAGC CAAAAGGACA GCTGAGGTTG ACATTGGCAC GAGCAGATGT 2820
CTAAGCTATA GACTGTCAGG TCTGGGGACG GGGGATGACT TTGGGACCTC TCAGTCCAGT 2880
CCTTCAAAGG CGGCTCGGTT CACAGGGGGC TGAAGGGCAG GGGAGTGTCA CTGCAGAGTC 2940
AAATATATCC GAGACCAGGG TCTGCTCTGC CAGATACTGG 2980