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

TagContent
EnhancerAtlas ID
HS197-09660 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr17:81038680-81042810 
Target genes
Number: 10             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs66468457chr1781041938hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr17:81042563-81042573GCCCCGCCCC+6.02
RREB1MA0073.1chr17:81039536-81039556CCCCCCCACACACACACACA+6.17
RREB1MA0073.1chr17:81039538-81039558CCCCCACACACACACACAGG+6.17
RREB1MA0073.1chr17:81042750-81042770TGGGTGCGGGTGGGGTGTGT-6.35
RREB1MA0073.1chr17:81039563-81039583CCCCCCAACACACACACACC+6.69
SP3MA0746.2chr17:81038943-81038956AAGGGGCGTGGCG-6.02
ZfxMA0146.2chr17:81041469-81041483GCCGGCTAGGCCTG+6.08
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_01998chr17:81037943-81043381Aorta
SE_23159chr17:81037451-81040668Colon_Crypt_1
SE_23159chr17:81040813-81043300Colon_Crypt_1
SE_23811chr17:81037428-81040409Colon_Crypt_2
SE_23811chr17:81040952-81041714Colon_Crypt_2
SE_23811chr17:81042141-81043347Colon_Crypt_2
SE_24692chr17:81036127-81044042Colon_Crypt_3
SE_26841chr17:81036543-81044451Esophagus
SE_27794chr17:81037891-81048100Fetal_Intestine
SE_28661chr17:81037871-81048127Fetal_Intestine_Large
SE_32097chr17:81036774-81040336Gastric
SE_32097chr17:81040491-81042910Gastric
SE_35080chr17:81037773-81040198HeLa
SE_35080chr17:81040687-81042659HeLa
SE_43234chr17:81037486-81043880Lung
SE_44287chr17:81038495-81046480NHDF-Ad
SE_45495chr17:81037917-81044052NHLF
SE_47794chr17:81040786-81041336Pancreas
SE_50617chr17:81037511-81043137Sigmoid_Colon
SE_52664chr17:81037540-81043347Small_Intestine
SE_57534chr17:81037501-81039971VACO_503
SE_57534chr17:81040814-81041715VACO_503
SE_57534chr17:81041845-81042920VACO_503
SE_58261chr17:81041086-81041579VACO_9m
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr178103868781040054
Enhancer Sequence
GGAGAGCCGT GGCCGGGCTG GCCCGGGCCT GGGTCCCGCT TCCCCTCGGC GCGGCCCCCG 60
CCCCCGCCCC CGCCCCCGCC GCGGGCCGAG TCACGCGGTG ATGTCGAGCG AAGCTGTTTT 120
CCGAGAAGGT CGGGGCAGAG CCGGTGCGGG GCGGGTGGTG TCCGCGGGGC GGGCGCAGGT 180
CTCCCCGCAG CCGCAGCCTC CGTTCCGGGT CCCCGCGAAG CCACAGTCGC CCCCCAGCGC 240
CCCCGGCGGA GCCTCCCCGG GGGAAGGGGC GTGGCGCTGG GGGGCAGAGT CGCCCCGAGG 300
GCCGTGGGCG GTGCCCGGCT GTCCCGGGAG CGGCCGCCTC CCTTCTCGGC CGAGCGGGGC 360
CGCGGGCGGA TGGAGGTCTG GGGGGGGTCG GCCGGGAACG CCGGCGCCGG GAGCCTCCGA 420
GGCCGACGGC TCTTCTGGGG CCGCCCCTGC CCCCGCGGAG TGATTCAGCC CCGGCTCGCT 480
GCCTCTGCCC GGCGGGTCGG TGCATCCCCG AACCGAGGCC CGGGGCGTTC CGCTCCAGCA 540
GACCGAAGCC AGAAACGCCG CCCCCGCCAC CCAGGCCGAG TGTGTCGAGA AGGGGCCGGC 600
GCCCTTTTCA GGGTGTCAGG GGACTGTGTG CCCGGTAGGA GGGGGCGCCT CCCGGAGCCC 660
GAAGGGAGGG CGCGGTAGGC AGCCGAGGGT GGCGGGGAGG CCACCCCTCC ACCTCCAGGG 720
GCGGGCGGCT CCTCCAGGCA GGTGACAGCA GCGGGACAGG AGTGCTTTGC CCTCCAGGAC 780
CTGCGCACCC TCCTGTCTAC CTGGAGGCCC TCTTCGCCAT CGTTGCCAGT CCTGGCCTCA 840
GACTCCCCAG AGGGGACCCC CCCACACACA CACACAGGGG ACCCCCCCCA ACACACACAC 900
ACCTGCAGAG CCTGGCAGAG GGCAGCTGTG GGGGCTGCTG GAGCTGCGGG TGTGATCTGG 960
AGGGGACACG GGGCCCGGCT GTGTTTCTGG GGCGTAAGTG AGACTTCCTT TTGTTGTGGT 1020
CACTGCCCCG TTGATCCACA CACGTCACGA ATCAGTGACA GAGACTCGCT GTGGAAACCG 1080
GAGTGCGCTG GCCTGCCTGC TACCCTCCGG TGTTTGTGAC TTTTTACCAG CTGTCCTGAC 1140
GAAGCACAGG GTGGAGCGAG CGCTGGTGTG CTGGGTGGAT TCTCATCCCC CGATAGCTGG 1200
AAAGTTGCCC CTCATGACAC TGGCCACTGC ATCGACGGCC TCTGTTGCTG GGTGTTTCTT 1260
CTAAGCAGTT AAGTAGGAGA TGATGAAACC TCCCTTCCGT GGGGGGAGGC GGGACCAGCG 1320
CCCCGTCTTT ATCAGCCAGT GCTCATAAAT GTGGACCATG AACTTTCCCA CTTGCTGTCA 1380
GCCCGGGCAT CGCAGGTGCG GTCACACCTG GTTCGTCTCT CCTGCAAGGT GGGGAAAGGA 1440
AAGTTAACCT GCCAGTGGGT TCGAAGCCCT TCCTGACTTT CATACAGGAG CCGGGCATTT 1500
TGTCCTGGTG ACCCAGAGTT GTGGTGTGTG GGCTGGTGCC TCAACAACCC TCCAGTGCAC 1560
CTGCGCCCCC CTTCAGTGAG TCCCTTTATC CACTTGGGAT TTGCCCTCCT TTCCATGAAG 1620
GTGCCCCACA AGCATGTCCA CCTGGGTGGT AACCCTTGCT GACTTTTAAA AGTGTATCTG 1680
TTCAGTCTGT TGATCCAACA TCAGATCAGC CTTGTCAGTT TCCTAAAGTT GAACGAACCA 1740
CGGTTTTGTC TGCACGCTTC AGTTTTATCA CAGCAGAACT GTGTCACCTG CATCTCACGT 1800
GAAAATCACA AAATGCCCTC ATCCATGACC ATTAAAGATA GGTCACATTT TTGCAATGCC 1860
AGCAATTTTG CATAAACAGA CTCTGTTTTC AGGTTTGCTG AGGTGCTGGA TATTTGGAGG 1920
TGAGAGATTT GAGGCACTCG ATTTTCTGGT AGGAACCAGC ACAGACCATG AGTCTCGGAC 1980
TTCGTGCCGA GGTCTGCTGG GTCCCAGGCT GAAGGATGCA TCGTTTAACT TTTTTTGTCT 2040
ACACGGGTCT TGCGCATCAT GTGCTACTGA TTTTAATGTG AAAATCCCTA CGTCAGCGGG 2100
TCTGGTTGGA GTCCCGTTGG TCTGGATGTT TCGGGAGAAT GTGAGAGGAG AGGGGAGCAG 2160
GCCCTGTGCT GGGTGCAGAC CCGTCTGAGT GCGCTGAGAA GACGTCAGGT GAAGGCCGGG 2220
GTAGCCGGGT GTCTTCTTTC TTCTGTGTCC ACCTTCATTT TGTCCTCTTC CTCTTTTTGC 2280
CCAGTGTCTT CTGAGTGGGT GGAGCCAGGC GTGCCCACCA GATGCGGGTA GCATGTGCTA 2340
GGCCAGGACG GCCCCCAGGC TCAAGTCGGC CTCCTCCTGG GCAGAGGTGG GTTGGCCGCC 2400
TGTCCCCAGC TGAGTTGTGG CTGTTCCCCT CGCCTGCTCA GATGAAGGCA GTGCTGTCAG 2460
AGGTGACCAG AGCCCGCTCC CTCGACCTTC AGGACTCCCC GAGAGGGAGG CAACGTGTCA 2520
GGACGGTGTA TGTGGAGAGA GGGTCGAGGC TCGGTGCCTG AGCACGGGCA GGAGGACAGT 2580
GGCCTCGATG CCAGAGACGG GAGGGAGAGA CGTGACGATG AGGCTGCATA AGAAGAGAGC 2640
TGACTGTAGC TGAGTGTATC AGCCACTCAC CGAGTCCAGT TTCCACACAG CACGATCATC 2700
GTGCCCTTGC CCACACACGT GTTAGATGAG CTTGTGTGAG CTTTATGGGC TGTAATTTGT 2760
GAGTCTGTTC TGGGTGTGTG ATCCTGGCAG CCGGCTAGGC CTGGCCACTC GTGACCTGGG 2820
GCCTTGTCGG GGTGGGGAGA GGGTGAGGAG GGGTGCACCC TCGACACCAC CCTCTGATGT 2880
GGCCTGCAGC CTATGAAGAG TGAGGTTTGG GGGCCCAGAG TGTGAGTCAC CAGCGGTAAA 2940
TGCAAACCAT ATGTGATGCA TTTTCTCTGC TGCAGAAAGG GTTTCTGGTG ACTCGCTCAG 3000
GCCAGGGCTC TGGAAACAGC ATTGCTTATT TCACATAAAA ATCCTAAGAA TGTGGGTGAA 3060
CCTGTCTGAG ATCTGCGTAA TAAAACACTT AGTTGAAGTC ACCGGGTTAG TTCCAGGCCC 3120
ACTTGGTTAT GACGTGGCTG TTAGCCACGA GCTGGCATTT ACGTTAAAGT GTTGAGAAGC 3180
GTGAGGGTTT TGATGTTTCA GTTTCTTGAA AATATAACTG TTTCTACTCA GGACCTGCCT 3240
CTCCAAGAGT GTAGCACACT TCATTTTTTT CTGTTTAGCA TGTATGAGGG TGAACTTAGC 3300
TTGCTACTCA CACACTACTC ACCCTGTGGA GGAAGTTCGC CTCGCTTTTG TGGTGAGTCT 3360
TGCTGTAATG ATAGCTTATA TTTACAAATA CCGTCGGCAG TGCAGGGTCT TCAGGCTTGC 3420
AGAAAACGGT CAAGTCATTA CTTTGAGAAA TGTACAAACA TCTATGCTTA ATGAGGTGCT 3480
AAAAGACAAA ACTCATCTAC AACCTCCTTC CCCCCAAACT GCCAACACTC TGGATTAACT 3540
TAAAAGCTGC TCTCTGGGCA GGTTGCATCC CAGGGCTCCT CCTTCACACG TGGTGGGGCC 3600
CCACCTTCGC TTTACCTCTA GCGTCCCAGC CCTCGTGGTC ATCTGGAACC AGGGTTGGTA 3660
CACAGGGCCT GCTGGCATTC CTGTGATACT CCGTGATATT CTGGAGGAAT CCATCCCTTC 3720
CCTGGGGCTC CATCCCACTG CCCCAGCACC TCCAGCCACC CTGATTCAGG GACATCGCAG 3780
AGATTGGTGT TTGACGCTAC GGCAGCAGAG GCGCAGACTC TTGAGTGTTG GAGGGTGTCT 3840
GGAGGGCCTG GGGACAAGCA CCGCCTGCAC TCCCGGGAGC TCGGCCCCGC CCCACCATGG 3900
CTCTTGGTGC AGGTGCACTG GAAGGAACTG GGTGGGGCCC TTGTGCCGAA GGGCGGAGAT 3960
GGCGCCGGCC TGCCTCACGG GCAGGGGTCC GTGTGGCACC TGTGGCCGGC AGCGGGTGGG 4020
TCCAGGAGCC GCCATCATTT GGAGCGGGTA TCGTCCTCAC TGACTCTCTG TGGGTGCGGG 4080
TGGGGTGTGT GACGGGAGCT CCGGGCCTGG CTGACAGTGT CTCTCCTCTG 4130