EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS115-02203 
Organism
Homo sapiens 
Tissue/cell
Kidney_cortex 
Coordinate
chr19:33531360-33534640 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10411210chr1933532300hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXP2MA0593.1chr19:33532688-33532699TTTGTTTACTT-6.62
Foxd3MA0041.1chr19:33531867-33531879AAACAAACAAAC-6.32
HES2MA0616.2chr19:33532960-33532970GGCACGTGCC+6.02
HES2MA0616.2chr19:33532960-33532970GGCACGTGCC-6.02
NKX2-3MA0672.1chr19:33533006-33533016ACCACTTGAA+6.02
RREB1MA0073.1chr19:33532089-33532109CCTCCAAACATCCCCCACCC+6.14
ZEB1MA0103.3chr19:33533183-33533194CCCACCTGCCC+6.14
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_23354chr19:33531310-33533037Colon_Crypt_1
SE_23354chr19:33533041-33533729Colon_Crypt_1
SE_23354chr19:33533969-33534304Colon_Crypt_1
SE_24632chr19:33531833-33532986Colon_Crypt_2
SE_24632chr19:33533052-33533609Colon_Crypt_2
SE_24867chr19:33531356-33533794Colon_Crypt_3
SE_27867chr19:33529698-33533862Fetal_Intestine
SE_27867chr19:33534149-33535156Fetal_Intestine
SE_28788chr19:33529691-33534092Fetal_Intestine_Large
SE_28788chr19:33534145-33535514Fetal_Intestine_Large
SE_32296chr19:33531754-33533737Gastric
SE_33901chr19:33530645-33533837HCC1954
SE_33901chr19:33533925-33535494HCC1954
SE_35571chr19:33529621-33533888HepG2
SE_42005chr19:33532234-33532844LNCaP
SE_42005chr19:33533043-33533521LNCaP
SE_47226chr19:33529418-33544806Panc1
SE_50977chr19:33531317-33533825Sigmoid_Colon
SE_52660chr19:33530653-33533813Small_Intestine
SE_52660chr19:33533949-33535437Small_Intestine
SE_56754chr19:33531354-33532337VACO_400
SE_56754chr19:33532345-33533023VACO_400
SE_56754chr19:33533064-33533657VACO_400
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr193353223833532582
chr193353184533532952
chr193353404433534233
Number: 1             
IDChromosomeStartEnd
GH19I033039chr193352963633535923
Enhancer Sequence
GTCTCGATCT CTTGACCTTG TGATTCGCCC ACCTCGGCCT CCCAAAATGC TGGAATTACA 60
GAAGTGAGCC ACAGTGCTCA CCGGCCCTGC TTTAAATTTC ACAAGGACTG CCTCAATTTC 120
AGATAAACTT CATCATATTT CTACCCTAGC TTTTCTCAAG GGAGGGAAGC TGGGAGAAGA 180
CAGAATATTG TCTCTGGTTG GCCTAAATGA AAAAGTACGG TCAGGCATGG TGGCTTACAC 240
CTGTAATTCC AGCACTTTGG GAGGCTGAGG CAGGCAGATC ACCTGAGGTC AGGAGTTCCA 300
GACCAGCCTG GCCAACACCG TGAAACCCTG TCTTACTAAA AGTATAAAAT TTAGCCAGGC 360
ATGGTGGCAC ATGCCTATAA TCCCAGCTAC TCGGGAGGCT GAGGCACAAG AATCACTTGA 420
ATCCAGGAGG TGGAGGTTGC GCAGGTGAGC TGGTATCTCG ACACTGCACT CCATCCTGGG 480
AGACAGAATG AGACTCTGTC TCAAAAAAAA CAAACAAACC TGAAAAAAGT GCATTTGAAA 540
TATTTGATGG CTTCCTAAAA AAACTCCAGG AAGCTCATGG ACTCCCAGCT GGAATGGATC 600
AGAGAAGGGG AAGACTTTGA AGGATCATAA AATCTGGTTT TTCAAGTGCC TGCCTAGCCA 660
CGATACCCTC TGACAGTCCT CAGATAAGGG CTTAGCACCC CCATTTCCAT TCCTGCATTT 720
CTGGGGACAC CTCCAAACAT CCCCCACCCC TATTCCAACA GATCTACTTT CCTTTGGGGG 780
CTGCGGTAGG AAACCTGGGA ACCAGAAGAC AAACAGAAGG AAAGCAGGGC CTAATTTACA 840
ACTGAAACCA CCCATGGCCT GCAGAGACAG CCACGTAATG GGTCGCCCAG GGACACTGAG 900
GGGCCAGAGC GGAGCTTGGC AAAATGCCCT ATTTGTTTTC GGGAAACCGT TGGTGCTTGT 960
TGAGTCAGAT TAATAAATAC CTTCAGGGTT TCCTCTGACA ACATTCTCCA GCAAGGGGTA 1020
CTTTGAACCT TTAGGCCACT GTGAGAATCA TTAACAACCC CCCACTCCTG CCCCTGCCAA 1080
CCCAACCACT GCCAGTTTAA CAATGAGCTT GAGTCAGGCT CGGGCCTCAG AAAGGGTGAC 1140
TGCTGTTGTC GTTAAGAGAA CAAGGCACAC AAAACTGCCC TAGTTCCTGC CTGAGAAAGT 1200
CCAAGTTCCC TGCTCACAGG GGCCTCTCTG ACCACCCTCT GTCTCTAAGG CTGGCCATCC 1260
TGGGCCAACC TCTATGATAT TCAGAGTTCA TTATTCCCTA GAAAACATCA CTTCCCTAGG 1320
TGATCTGATT TGTTTACTTG TCTATAAAAG TCTCCTCCCA TCCTCCAACA AGAGAAATCA 1380
CAAAAGCAGA GCCTCGCCTG ATCTTCAGGC ACCTCAACTG TGCCTGCCAC TTAACAGGTG 1440
CTCAATAGCC AGGCACAGGG GCTCACTCCT GAAATCCCAG CACTCTGGGA GGCTGAGGCA 1500
GGAGGATCAC TTGAGGCCAA GACTTTGAGA CAAGCCTGTG CAACACGGTG AAACCCTGTC 1560
TCTACTAAAA CTTTAAAAAA TTCAATTAGC CAGGTGTGCT GGCACGTGCC TGTAGTCCCA 1620
GCTATTTGGG AGGCTGAGGC AGGAGAACCA CTTGAACATG GGAGGCAGAG GTTGCAGTGA 1680
GCCAAGATTG AGCCATTGCA TTCCAGCCTG GGCAACAAGA GTGAAACTCC ATCTCAAAAA 1740
AAAAAAAAAG GTGCTCAATG AATCCATGAA TAGGTAAATC AATTGTTGTC CACTCCTAGG 1800
AAAGCCATAC ACCATCAAGG CTGCCCACCT GCCCCCTTGG CCACAGAGCA GGCCTGTCCA 1860
AGGGTCAACC AGAACCCTAG GCCACAAAAC ATACCACGGC CTTCCCAGCA CATGACAGGG 1920
AGTCCCAAAA TCGGGGGCCT CTCTCACGTC ACACAGATGA CATGAGTTGC TCTCTGCTAT 1980
GGGAGTGGAC AATTCCCATG TCCAAACTTG TCTTGGGATA GGGACACTGC TTGACTTTTT 2040
AAAAGCCAAA ACGCTACAGT ATTTTTCCCA GCCTCCTCCA GTAACAACCT GCTTTGCACC 2100
CAGTTGCAAA AGGAGCTGGA GAAGAGATTC CCAGACAAAC TTCCCACCCA GGACCTCAAG 2160
TCATCAGGTA TTCCGTGAGT AACAAAAGCA ACACAGGCCA GGCACAGTGG CTCATGTTTG 2220
TAATCCCAGC ACTCTGGGAG ACCAAGGCAG GAGGATCACT TGAGGACAAC AGTTCGAGAA 2280
CAACCTGGGC AACACAGCAA GACCCTGTCT CTACAAATAA TTTTTAAAAA ATCAGTCGGG 2340
CATTGGCCAG GCACAGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CTGAGGCGGG 2400
TGGATCACGA GGTCAGGAGT TCGAGACCAG CCTGGCCAAG TTGGTGAAAC CTCGTCTCTA 2460
CTAAAAATAC AAAAATGAGC CGGGCACGGT GGCGGGCACC TGTAATCCCA GCTACTGAGG 2520
AGGCTGAGGC AGGAGAATCA CTTGAACCTG GGAAGCAGAA GTTGCAGTGA GCCAAGATCA 2580
CGCCACTGCA CTCTAGCCTG GGTGACAGAG CAAGACTCCG TCTCAAAAAA AAAAAAAATT 2640
AGTCGGGCAT GGTGGTGCAT GCCTGTGGTC CCAGCTACTC AGTAGGCTGT TAGGAGGATT 2700
GCTTGAAGAG CCCAGGAGGT TGGGGGCTAC AGTGAGCTGT GATTGCACAT TGCACTCCAG 2760
CCTGGGCAAC AAGAGCGAAA CTCCATCTGA AAAAAAAGAA AAAAGGTGGC ATGACGCCAG 2820
ACGCAGTAGC TCGCGCCTGT AATTCCAGCA CTTTGCGAGG TGGAGGCAGA CGGATCACTT 2880
GAGGCCAGGC GTTCAAGACC AGGCTGGCCA ACATGGTGAA ACCCCGTCTC TACTAAAAAG 2940
ACAAAAAATT AGCCAAGCAT GGTGGTGCAT GCCTGTGGTC CCAGCTACTG GGGAGGCTGA 3000
GGCAGGAGAA TCACTTGAAC CCAGGAGACA CAGGTTGCAG TGAGCCGAGA TCACGCCACT 3060
GCACTCTAGC CTGGGCGACA GAGCAAGACT GTCTCCAAAC AAACAAAAAA CAAGGCGGCA 3120
CGGGGCTAAC CATGGTCTCC AGTAGAACTC TGAAGGAAGA AGAAACTCTG CACTCTTTGT 3180
AAACAGAGTG CTGGCACATT GTCTTTTGTT GCATTTCGTT GCCTGGAGAG GGTTTATAGA 3240
GGTCTAGACA CAGGTAAGGC TTCTCTGAGT TCTATGCTGG 3280