EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-36414 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr17:81058850-81062900 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs75954926chr1781061048hg19
TF binding sites/motifs
Number: 15             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr17:81060350-81060360GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060382-81060392GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060413-81060423GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060477-81060487GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060509-81060519GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060541-81060551GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060571-81060581GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060602-81060612GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060697-81060707GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060728-81060738GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060759-81060769GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060791-81060801GCCCCGCCCC+6.02
KLF5MA0599.1chr17:81060823-81060833GCCCCGCCCC+6.02
PLAG1MA0163.1chr17:81061314-81061328GAGGCCAAGGGGGG+6.06
ZNF263MA0528.1chr17:81059132-81059153TCCCCAGGCTCCTCCTCCTCC-7.08
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_01998chr17:81058746-81060371Aorta
SE_01998chr17:81060848-81063603Aorta
SE_23159chr17:81058726-81060419Colon_Crypt_1
SE_23811chr17:81058799-81060091Colon_Crypt_2
SE_24692chr17:81058755-81061266Colon_Crypt_3
SE_24692chr17:81061731-81062425Colon_Crypt_3
SE_26841chr17:81058765-81061145Esophagus
SE_27794chr17:81059812-81060477Fetal_Intestine
SE_32097chr17:81058901-81060299Gastric
SE_35080chr17:81058816-81061950HeLa
SE_43234chr17:81058821-81060455Lung
SE_43234chr17:81060691-81062567Lung
SE_44287chr17:81058879-81060315NHDF-Ad
SE_44287chr17:81062120-81064768NHDF-Ad
SE_50617chr17:81058789-81060926Sigmoid_Colon
SE_52664chr17:81059172-81060261Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr178106096881062367
Enhancer Sequence
GGTGGACAAG GGTGGCAGGA CCTGTGAGAT GATGTGAGTG CAGCACAGTG GGGCTCTGTA 60
AGAAGCGACC CGGGCAGCTT GAGCAGGGGC AGGCTGGGCG GTGCCTACGG GTCTCTGTCC 120
ACCGGAGCCT CTGTTCAGCC CACCTCAGTG TCGCTCCGGA TGTGGATAGA AGGAGACACT 180
GCCTGGGCCA CAGACCAGGT GCTTCCTTCG TCCTGACCAC ACCTGCTTCT GCCCAGGAGA 240
CGCTGCAGGG GCTGTGCTCC CCGCCCGGCT ACTCTTGAGT GGTCCCCAGG CTCCTCCTCC 300
TCCCGGTTCC ACCTGGAGCT GTGGGGCTGT GCCGGGGATG CCTCGCTGCA GCTGCAGCTC 360
AGGGAGAACT CACTGCTGGA GCTTCTGCCT CTCCCGTGCC GTGGGGCCGA GCCGAGCTCC 420
ACCAGGGTCT GGACTTCTGC ACGGGCAGCT GTGCTTCCCA GGGTCGTGGA GAGGGGTCCT 480
TGGTCCCAGC CACTGTGTGA CCTCGACCAG GACACTTGAC TTTCCTGCCC CCAGAGGGTC 540
TTGTCTGGAC CTCCAGAGCC CCCAGCCTTG CTCACTTGGC TCTGCTTCTG GGCAGGGTGC 600
CCTGGCATTG CTGTTGCTGG CACCTGCCGT GCCTTGGAGG GGTCTCCAGT GGGACCTCTG 660
AGCACGGCTC TTCCTGTACT TCTCAGAGGT GAGCAGAGGG CATTTGTGGG AGAACTGGAA 720
CCTGGGGAGG AAAAACCCCA AGGCTGGCAA AGACTCCCTG CAGTCTGTCC AGTGATCCAC 780
TGAGGCTGAG TGGTGGAGGA CATGGAGGCC GGCCCGGGAC CAGGACATGG AGGCCGGCCA 840
GGGACCTGGG GAAGAGAGGG CCTCAGTCTG GTGAGACCAG CCTGGTGGGT GCCTGGGGAA 900
GAGAGGGCCT CAGTCCGGTG AGACCAGCCT GGTGGGTGCC TGGGGAAGAG AGGGCCTCAG 960
TCCTGTGAGA CCAGCCTGGT GGGTGCCTGG GGAAGAGAGG CCCTCAGTCC GGTGAGGAGA 1020
CCAGCCTGGT GGGTGCAGGC CACCCTTGCC TGCTGTCAGG GCCTGCCCTT CTCTCCGGCC 1080
TCCAGCTGCT TTGCCCCAGC GATCAGGCGC CTGAGCTTCC TCCCCCGAGC CTGAGTCCAG 1140
CTGAGCTCCG TGTGGCTTTC CCGGTGGAGC AGACTCTGTC TGATTTCCCG ACGGCTGGCG 1200
CCTCCACCTG CTTCCCAAAA CCGAGCACCA GGGGTCTGAG AGGTTGCTAT GGGAAGGTCG 1260
CTTGCTCCAG GGGGCCCTGG AACAGTTGCT AAGTTTAACG CCCTGGCCCA GGATCCACCT 1320
GTCCTGCTGC AGACCAGCCC TGCTCATTCC TCCCTCTGGC TGTGAAGATG GAAGCCCATG 1380
GGTTGGATGC CTCGGGCCAG GGCTGTCACG CAAGGAAGCC TGGGGAGGAC TGTGGCACTG 1440
ACCCCATGGG CCATGGTATC GCCTCAGGGC CCTGCCCCTC TGGATCTCCG TCTCCTCAGG 1500
GCCCCGCCCC TCTGGATCTC CGTCTCCTCG GCGCCCCGCC CCTCTGGATC TCGTCTCCTC 1560
GGCGCCCCGC CCCTCTGGAT CCCTGTCTCC TCGGGGCCCC ACCCCTCTGG ATCTCCGTCT 1620
CCTCGGCGCC CCGCCCCTCT GGATCTCCGT CTCCTCGGCG CCCCGCCCCT CTGGATCCCC 1680
GTCTCCTCGG CGCCCCGCCC CTCTGATCTC CTCTCCTCGG GGCCCCGCCC CTCTGATTCC 1740
AGTCTCCTCG GCGCCCCGCC CCTCTGGATC TCCGTCTCCT CGGCGCCCCA CCCCTCTGAT 1800
CTCGGTCTCC TCGGCGCCCC ACCCCTCTGG AGTTCCGTCT CCTCGGGGCC CCGCCCCTCT 1860
GGATCTCGTC TCCTCGGCGC CCCGCCCCTC TGATCTCGGT CTCCTCGGCG CCCCGCCCCT 1920
CTGGATCCCC GTCTCCTCGG CGCCCCGCCC CTCTGGATCT CCGTCTCCTC GGGGCCCCGC 1980
CCCTCTGGAT CTCCGTCTCC TCGGGGCTCC GCCCCTCTGA TCTCCTGCAC GCACCCGGCC 2040
TCGCCTGAAA AGCCCCACGT ACAGCAAAGC GGCCGTGTCT TGGTGGCCTC TGCCTGGGGC 2100
GCTATGGGTG GCCTGTCTAT GCCTCAGTTT CCCCATTCTT GATGAGAGGG AGCTGGGGTC 2160
GCTACTGGTC ACTCGGGCCC CAGGCAGACC AAGGCTCACT TCTGTCCACT CCCTGGCCCC 2220
ATTCCCAGGA ATCCCACCGG TTCCTGGCCG GGGTCTGGAA TCTGTTCTCC CAGTCCAGGA 2280
CCTACCCTCC CCTCCACTTC CTGCCTGCAA GCTCTGTGGT CCTTCCTTGT CTTGAGTCCA 2340
GGGTTCCCTG TGCTCCCAGT CCAGCCTCCC TACTCAGGGC CGAGGGCACC AGGAGGATGG 2400
TCGTTGCAAA AGAATATGGG AGGCCGGGTG CGGCGGCTCA CGCCTGTAAT CCCAGTACTT 2460
CTGGGAGGCC AAGGGGGGCG GATGACTTGA GGCCGTGCAA CACCTGCCAG CACCAGCATT 2520
TGACACGGAA TCGAAGAAAA CAGGCAGGAC ATACCCTGAC TACACTAGTA CAAGTCATCG 2580
GCGTCTCGGG GTCCTGGGTT TTAGAAATCA CACTGTCAGG GAGGGCTGAT GGGGTCCTGG 2640
GTTGGAGGCT GGAAGTGGAG GAATCGAGGC ATAGGCAGAA ACTTGAAGGA AGGGTCAGCC 2700
GAGCTGGCCA GAAGGGGGCT CCTCGCCACG GTCCCCAGGG AAGCACTTTG CTCATGGGCC 2760
CCGGCCCTGA GAGAGGAGCT CCTGCCTCTT CCCACTCGGA GAGGGCTGAC AGGAGAGGCT 2820
TGGCCTGGTG TTTCCTGATG AGATAGCGGG CACGTTCCGG GAAGCGGTGA GCAGGCCCAG 2880
CAGACATCAG ATGTGGTGCT TCCTGTCTCC TGTGAATGCG CCTGGCCCTT GAGGGGGGTC 2940
TGGGATGGAG AGTCGGGGGA GGGGAACCCC ACTCGCCCTT CTCCTTGTTG TTCTTGGCAG 3000
CTGGACTTGG GCAATTGTGC CTCCACCCTC TGGAGGGGCC TCCCCCTGTG CTGGCTGCAG 3060
ATCAGAGGGG CGATGGGGAG GGATCCACCG GTCCAGGCGG GGGCTCACCT TCCAGACCCG 3120
GGCGTGGGCG AGAGGGGTGC ATGGGAGGAC GCCCGATGCC TCAGGGCCCC CGGTCAGCAG 3180
CGAGGCACAG ACTCTCCTCT GGGCGGTGAT GGCCCTGCAC GAGGTCCGTG TGCCGTCTGC 3240
CTGCACAGGG AGAGGAAAGG ATCACGCGAC CATGGGTACG TTGGCCACCT GAAGGTTGAG 3300
TCCCGCAGCC TAGAGACTGG AGCGTGGGGA CCAGGAGGAG CTTCTTAGCG GAACTGGGCT 3360
GGGGCTCATG CAGCCCTCCA GGAGCCCCCG ACGCGACGCC CTGGCTCATC CCGGGTGAAG 3420
AGGCTGCTGA GTCTGAACTG ATGACAGTGG ACGGGTGGCC GCCGGTTCCC AACGCATGGT 3480
TGGGCCTGGA ACCCAGGTGA CTCTGGGAGA TGTGGTCACA GTCACAGCCG TCTGTGGGCC 3540
TTTGGGTTCA AAACAGCGCG AGTCACAGGA GACAGAAGGG AATCTGAGCT TGCGATTGCT 3600
CATTCTTGTC ACCCTCCTGG CTCTGGGACA CCTCTGCCAT CTCCTACCAA GGGTACCCCA 3660
TTCCTGGCGA GTTGGAAAGT GGCCTCATGG GCAGAAAACG AGGGCAAAGG GAGCTGCGTG 3720
CTGTGAGAGA CGTCCCCGCA CCCACCCTCC CCACCAGCTC CCTTGGGCCT TTCCTCCCTC 3780
CCAGCCCCAC CCACAGCCGG GTGGCTCCCT TCACTGTCTC TCCTGGGTTT AACTCAGAGG 3840
CTGGCGAGCA GGGGCTGACC AGTGTGTGTC GGAGACTCTC CGAGTGGCCA GCACGGGCAG 3900
GGAGCTCATA GGCTTGGCCC TGAGACCAGG TCCTGTCTGA GAAGGAGGCA GGTCCTGTCT 3960
GAGAAGAAGG ACCCCCACCC CTCCTGCCTG GGACCCTGCC TTAGGCTCAC TCTAATGACC 4020
TAATTTCAAT TTGATTGAAT GCAAATCTGA 4050