EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS194-00012 
Organism
Homo sapiens 
Tissue/cell
Urothelial_cell 
Coordinate
chr1:9340300-9342670 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs916379chr19341128hg19
rs677665chr19341786hg19
TF binding sites/motifs
Number: 32             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr1:9340448-9340459GCCCCGCCCCC+6.02
KLF16MA0741.1chr1:9340466-9340477GCCCCGCCCCC+6.02
KLF16MA0741.1chr1:9340484-9340495GCCCCGCCCCC+6.02
KLF5MA0599.1chr1:9340448-9340458GCCCCGCCCC+6.02
KLF5MA0599.1chr1:9340466-9340476GCCCCGCCCC+6.02
KLF5MA0599.1chr1:9340484-9340494GCCCCGCCCC+6.02
RESTMA0138.2chr1:9341495-9341516GGCACTGTGCCTGGTGCTGGG-6.31
SNAI2MA0745.2chr1:9341181-9341191TGCACCTGTT-6.02
ZNF263MA0528.1chr1:9342505-9342526CCCTCCTTTTCCTCCTCCTCC-10.05
ZNF263MA0528.1chr1:9342541-9342562TCCTCTTCCTCCCCCTCCTCC-10.45
ZNF263MA0528.1chr1:9342567-9342588TCCTCCTCCCCCTCCTCCTTC-11.07
ZNF263MA0528.1chr1:9342558-9342579CTCCTTGTCTCCTCCTCCCCC-6.05
ZNF263MA0528.1chr1:9342582-9342603TCCTTCCCCCTCCCCTCCTTG-6.14
ZNF263MA0528.1chr1:9341728-9341749GGAGCAGAAAGATGAGGAAAG+6.18
ZNF263MA0528.1chr1:9342588-9342609CCCCTCCCCTCCTTGTCCTCC-6.54
ZNF263MA0528.1chr1:9342577-9342598CCTCCTCCTTCCCCCTCCCCT-6.71
ZNF263MA0528.1chr1:9342517-9342538TCCTCCTCCTCTCCCTCTTTT-6.75
ZNF263MA0528.1chr1:9342571-9342592CCTCCCCCTCCTCCTTCCCCC-6.82
ZNF263MA0528.1chr1:9342511-9342532TTTTCCTCCTCCTCCTCTCCC-6.92
ZNF263MA0528.1chr1:9342538-9342559TCCTCCTCTTCCTCCCCCTCC-6.98
ZNF263MA0528.1chr1:9342529-9342550CCCTCTTTTTCCTCCTCTTCC-6.99
ZNF263MA0528.1chr1:9342523-9342544TCCTCTCCCTCTTTTTCCTCC-7.16
ZNF263MA0528.1chr1:9342594-9342615CCCTCCTTGTCCTCCTCCTCT-7.5
ZNF263MA0528.1chr1:9342544-9342565TCTTCCTCCCCCTCCTCCTTG-7.63
ZNF263MA0528.1chr1:9342532-9342553TCTTTTTCCTCCTCTTCCTCC-7.76
ZNF263MA0528.1chr1:9342526-9342547TCTCCCTCTTTTTCCTCCTCT-7.83
ZNF263MA0528.1chr1:9342502-9342523GCTCCCTCCTTTTCCTCCTCC-7.98
ZNF263MA0528.1chr1:9342570-9342591TCCTCCCCCTCCTCCTTCCCC-7.98
ZNF263MA0528.1chr1:9342591-9342612CTCCCCTCCTTGTCCTCCTCC-8.22
ZNF263MA0528.1chr1:9342508-9342529TCCTTTTCCTCCTCCTCCTCT-8.4
ZNF263MA0528.1chr1:9342564-9342585GTCTCCTCCTCCCCCTCCTCC-8.7
ZNF263MA0528.1chr1:9342535-9342556TTTTCCTCCTCTTCCTCCCCC-8.87
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_23490chr1:9337921-9342330Colon_Crypt_1
SE_23818chr1:9337980-9341807Colon_Crypt_2
SE_23818chr1:9341834-9342316Colon_Crypt_2
SE_24876chr1:9337785-9342445Colon_Crypt_3
SE_45049chr1:9340486-9342190NHLF
SE_50208chr1:9338047-9342398Sigmoid_Colon
SE_65576chr1:9340212-9341781Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr193404889341044
chr193410909342382
Number: 1             
IDChromosomeStartEnd
GH01I009278chr193384619342291
Enhancer Sequence
CTCCTGGAGT CAACCTTTCA TTCATTCATT CATTCAGCAA ATGGCAGTCG TGGGGTAGGC 60
AGCCATGCAC ATGGCAGTCA AGGCCCTCCC TTTCCATTCC AGACTGTGAT TGATCCGTGC 120
TCCCCTCCCC GCCCCGACCC CACTCCCCGC CCCGCCCCCA CTCCCCGCCC CGCCCCCACT 180
CCCCGCCCCG CCCCCACTCC CCGCCCCGCC GCTGGCAGCG GGCAAGGACC CACGACTCAT 240
CCCATGGCCT CCCTCTGGGT AAGTGCTTGT CGACTGAGTC AACGACTGAA TCAGCCGCGG 300
TTGTCAGGGC TCAGCTGGAC TGAGCGCTGC TGCCTGTGGG CGTTTCCTCC TCATGTGTTT 360
TTTATCAGCA GCAGCGGCTG CAGGGTCCCC GTGCTCAGGG GTTGCCTCTG TCGTGCTCAC 420
TCTGCCCCGC GCTCTGTCCA CACCCCTGCT CCATCCAACT CGCAGATGGA GCGGTTTCCT 480
TTGAGCCCCA GTCCTGTCCA AACACACATG GGTGCTGGGC TTTCCCTGTG GCACATTTTC 540
TACCCTCTGT AGGCAGGAAA GAGCAAGCAC ATGGAGGCAG CCCTGTTGTC CTTGGCCTTT 600
CCAGGACACC TGGGAGGAGA CAGCACCCTG TGAGGCTAAG AGCTGGACTC TGGAGTCAGA 660
AAGGTCTGAG TTCAAATCCC ACCCCTGCTG CTGAGAGAGT GGCACAGGGC AGTTTCACCA 720
CTGTGAGCTT GTTCCTCCTC TGTGAACTGA ATAATAAACC CTGCTTTCCA GAAAAGAGGC 780
GCACAGAGAG GACTTTATCA TAGGGCCCAC GATGAGCTCC CGGGGTCCGA GCGAGAGACC 840
CGCAGCACCA CTTGGTGGGG GCAGGGCCGT GTGTCTGCAT GTGCACCTGT TCATCTGCCC 900
ACCGCAGGCT CTCACATACC AGGGCTTTGT CTTCTGCAAG GATGACCAAG ACATGGCCCT 960
GCACTCAGGA AATGACAGGC AAGGAGCGTT CTCAGGGGTG GCAGATGTAG CGAGAGCACT 1020
TGGGTCGGAG CCACAGGGCT CTGGGCAGAG ACTGCGGTTC CGTGTTGGGG GAAGGAGGTT 1080
AGGGAGTCAG GAAAGATCTC CATCATGTGG GGGCCTTGAA TTAGAAGTTC AGCAAGTGCC 1140
ACAGACTGAT TTCACATCCC ACCACAAGTA TTTATTGAGC ACCTATTGTG TAATAGGCAC 1200
TGTGCCTGGT GCTGGGATAC ACGGGGTGGT AGCACAAAGG AAGACACTGC CCAGGGCTCC 1260
TGGCCTGGCG GGGACACAGA CAAGGGCCCA AGGGATGGCA GCCCCAAGGG GCAGGGCCAA 1320
GCTGGGCCAT GCGGAGGGTG CCGTGGGACT GCCTGGCAGG AGCATCTGTC CACCCTGGGG 1380
ATCAGTGCAG AACGTGATTC CATCCTGATG GAAAAGACGT TTCGGCTGGG AGCAGAAAGA 1440
TGAGGAAAGC GCTGCTGTGT GGCATGGGGC CAGCTGCTTC CCCTCCCTGA GCCTCGGTCT 1500
CCTCACCCAC AAGCGGAGGG ACTTGGAGCT CTGCTCTCTC AGGTTCTGGT GGCTCTGATG 1560
GGATGTGACA CCCATGACAT TCCCAGGAGC TGAGAGGATC TCCTGCTACT TGATAACCTG 1620
GAAGGCCCGT GAAAGCTTAG GGCTCTGTCA ATGTAGGAAT CAAGGCTGTG GAGGCAGATT 1680
AGCAGCAGTC CAGCCCCGAG CTGGGACCTG CTCAGCACGC CTCCTCTGCA CTGGCATTGC 1740
CTGCATGTCC AGGTCCTGCC ACAACTGCAC ACTCCACCTC CCAGCTCGAG CCCCGGGGCC 1800
CTCTGAGAGG AGGCAGAGCT TCTCTCTTGG TCTTTGCTGC AGCTCTGCAC CCTCCCCAGC 1860
CGGCCCAGGA GCCAGATGGG ACCCGGCCGA GCTGCAGAAC ACCGTGCACC TTCCTGCAGT 1920
CCTCAGCCTG GGACCTGAGG AGCACAGGCT GATGGCCTGA TGCGGCTTCC AGACAGAGCT 1980
CAGCCCACTC TTGGGAGGTG CCAGCTGCCT GGGTGGTCTG GTATCGGAAT GAAATCCAGA 2040
GGCCAGAAGG AGCCCAGGGT TCAAATTGCC ACCAATTTCC TGAAAGTTCC TCTAGAGCTC 2100
CGGGCAAACC CACCAGTTGA TTGCGGAAAA TAACAGACCC CTCACTTAAA ACCAGATGTC 2160
AGCATCTGTC TTGAACCAGC CCAGGGAGAG ACAGAGGCCC CTGCTCCCTC CTTTTCCTCC 2220
TCCTCCTCTC CCTCTTTTTC CTCCTCTTCC TCCCCCTCCT CCTTGTCTCC TCCTCCCCCT 2280
CCTCCTTCCC CCTCCCCTCC TTGTCCTCCT CCTCTCCCCC TTCCAACTCT GCAACCAGGT 2340
CAACCACAAC CTCTGGCCAC ACAACAGACC 2370