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

TagContent
EnhancerAtlas ID
HS115-00670 
Organism
Homo sapiens 
Tissue/cell
Kidney_cortex 
Coordinate
chr10:134220010-134223520 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs74383458chr10134221545hg19
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GabpaMA0062.2chr10:134221557-134221568CCGGAAGTGGA+6.32
PLAG1MA0163.1chr10:134223204-134223218GGGGCCAAATGGGG+6.75
RREB1MA0073.1chr10:134223129-134223149TCACCACCCACCCACCCACC+6.38
RREB1MA0073.1chr10:134223145-134223165CACCCACCCACCCACACCTC+6
RREB1MA0073.1chr10:134223133-134223153CACCCACCCACCCACCCACC+7.33
RREB1MA0073.1chr10:134223137-134223157CACCCACCCACCCACCCACC+7.33
RREB1MA0073.1chr10:134223141-134223161CACCCACCCACCCACCCACA+7.33
TFAP2AMA0003.3chr10:134222187-134222198TGCCTGAGGCA-6.02
ZNF263MA0528.1chr10:134223272-134223293TGAGAAGGAAGGGAAGAGGGG+6.29
ZNF263MA0528.1chr10:134221992-134222013GAGGGAGGGGCGGGAGGAGGA+7.74
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00873chr10:134218800-134226717Adrenal_Gland
SE_02964chr10:134220377-134223463Bladder
SE_04410chr10:134220363-134222950Brain_Anterior_Caudate
SE_09804chr10:134220280-134222532CD14
SE_10426chr10:134221360-134222162CD19_Primary
SE_11568chr10:134220135-134222912CD20
SE_23061chr10:134219282-134226762Colon_Crypt_1
SE_23725chr10:134219686-134223556Colon_Crypt_2
SE_24681chr10:134207224-134228585Colon_Crypt_3
SE_26753chr10:134219639-134228593Esophagus
SE_28153chr10:134220141-134223109Fetal_Intestine
SE_29112chr10:134220142-134223149Fetal_Intestine_Large
SE_31406chr10:134219015-134228553Gastric
SE_33290chr10:134220340-134223251H1
SE_34405chr10:134219619-134223123HCT-116
SE_41567chr10:134219041-134226713LNCaP
SE_42252chr10:134219499-134237674Lung
SE_47467chr10:134219234-134226760Pancreas
SE_50143chr10:134219172-134226712Sigmoid_Colon
SE_53287chr10:134219205-134237202Spleen
SE_56893chr10:134220205-134223564VACO_400
SE_57427chr10:134220150-134223273VACO_503
SE_57946chr10:134219984-134223521VACO_9m
SE_61428chr10:134196155-134334764Toledo
SE_65264chr10:134210665-134236634Pancreatic_islets
SE_68705chr10:134218519-134226778H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr10134221496134221692
chr10134221970134222202
chr10134222000134223200
Enhancer Sequence
GCCACCGCTG GTGCTTGTTG GAAGCACACA GCGAGTTTGT GTTTGGCAGC CATTTTTCAA 60
AGGCCGGAAG GGAGCTTCTC ATGCTCTCAG TCGTTGTTTG GAGTCAGGGA TGTGGTTTGA 120
CGGATCCTGG GGAGGGGAGA GCCCAGGCTG AGGCCCTGTC TTGCGTTACT CACTCAGGGA 180
ACAAACTCTC ACTGCTCTTT CCAAAGATCA GAGCGGGCAT CTCCCTCCTC CTGCACGCGG 240
ATAGGCCATC CCAGGACATT AAAGGAGGGA GGGCGAGGTG AGCTTCCCAC CCTCAGATGA 300
AGCCCCCACC CCAACTCCCC AGACTGGCCC AGCCCTGCCC CCTGTGACCC CCCAAATCTT 360
CCTCCTGGGT CAGTGCGCAC TCCGTCGTCA GCAGGCTGTG TGCGTGGCCA GGCGCCCGGG 420
ACCTGGGACA TGGTGTGGGG GCCTGTTCCC GGGGACGGCG TCTCACTGTC GGCCTCTACT 480
ACGAGCACTT TCTAGAATCT CCAGCCAGGC CTTGTGTGGA TTCTCTGTGC CTGGGGGGCA 540
CTACGCTGTG TGGAGGTGTG GGGGTGTCAC CTTGTGGGGC TGGGGGCACC ACCCATGCCC 600
CTGTAATCAC CACGTGGGGC ATCCGGAGCC TGCCGAGGGG CTGTTTTCTG CCCTGAGCTC 660
CTGAAGGCCA CTCTCCCAGC TCCAGAGGCC TTCTCAGCAC CTCCTAGATG CCCCTCTTGT 720
CTTCCCAGCA GGAGAAGGCA GGCCAGGGAG CAGTCCTTTC TGGGTGGGGG CAGCTGGTGG 780
CCCTCTGTGC TCTTCTTCCT GGCTCCATGG CCTAACCACC CCATGGATGC AGAGATTCCA 840
GGGCCAGGGG CTGTACGCAG AGGGCAGGGG CAGGGCTCCG CCTAGGCCTT GGTGACGTCT 900
GGTGACCTTG TCTTCCCTGG CCACCTGCCC AGAGGCCTTA GAGTTTCCCA GGTGACCGTC 960
CTCGGGCCTT TGTTGGGGGC GGGGACTGGA GCGCCTGGTG CCCCTCCACT GCTGCACCCT 1020
GCGTATTGGG GTTCCGGCGG AAGCAGTGAT GAGAGACCAC TGTGGTTGAG CCAGGGTCCC 1080
CAGGGTCCCC AGGCTGCCTG GCTGCCCAGG CTCTGGCCTG GCCTCACCCC CTCCCTCCAG 1140
CCACCCGGCT GCATCTGCCT TGCTCTCCTG AGGCCAGGCA CAAACCTGGC TGCTCCCCCC 1200
GCCCCAGGAA CCAGGCCCTT TTCTGATCAG TTCTGGGGCC TTGGGGCAGG CGTGGGGCAG 1260
GTGCCTTGTT GGCGAGTGGG TGTGGGTGCC GTCTCTCAGC TTGAGTCTGG GGAGTGTCTC 1320
AAGCCAGGGC ACCATCTTCT GAGGGGTAGG AGGAGGGTCA GAGGACTCCC GTCTGCTGTC 1380
CTGGGGGGCC CTCCCCGAGT TCTGGACTCA GGCATTTGCG AGGCATGACA TCCCCCCACG 1440
CAGGACGTCT CCAAGTGAGG CCTGAGGCCT TGGCTGGCAG GGAGTGCCCA GCCGGGAGGG 1500
AGGACGGGAG GACACAGTCT TGCAGGCTCA GGGCCGGCTG TGTTTATCCG GAAGTGGAGG 1560
AAGAATCTCA CCAGACGGGT TTGCCTGCCT CCACGGGGGG CAGTGCCTGC ACACGGGGCC 1620
TGCGCCGGGA CCAGCCCCCT GCTCTGGGAG TGGGGGTGCC GGATCCTTTC AGCACCAAAG 1680
CGCAGAGTGG TGTGTGCCTG GTTGGCTTTT TGGTCTTATT TCCTGAGGGC TAAAGACCAA 1740
GTGCTCAGTG TGATCAGAGC TGGTGTCTCG TGGGGCCTGG GATCTCCCGC CCTCTGTGGG 1800
GTTGGTGGTC CTTGAGGGAC ACGTTTGCTT TGAAGTGTCA GCAGCGCACC TCTGGTCTGC 1860
TCTTTGTAGG GGAAATGCGG GGGTACCTGC CTTTCCTGGG AAGGGGGACC CGCCACCACC 1920
ATCGTGAAGG CGCCTCTCTG AGCAGAGGCT GAGTGAGGTG TGGGGCGCTG CTGGCCATGC 1980
CCGAGGGAGG GGCGGGAGGA GGAGGCTGGT GTGGGGGCTG GAGCTCGGGC AGGGAGGCCT 2040
TCCGGGGAAG GTCGTCCTCC CAGCTCCCGC CCACCGGCCA CCCTGGCCTG GCCCCAGCCG 2100
CTCCTGCAGC TGCCCGAGGA TGAGGACGGG GATGGCTGGG CGGTGTCAGA AGCTTCCTGA 2160
GGTTTGTGGG TGTCTGCTGC CTGAGGCACT TGTCAAGGAG CAGTCACCGC AGGCACCACG 2220
AGATCGGCTC CGTTGCAGGG ACACTGAGCC CAGCATCTAC CCATGAGAGA CCCCTCACTC 2280
TCTCTCAGCT TGCTGCGGGG CTGGAGGCCC TGCTCAGGGG TAGGCGGATG CCCCACAGAC 2340
CACAGGGTGC CAGGGCATTG GGCCTGTGGC CGGCAGTGCC AAGAGGCAGC CTGGCTGGCA 2400
CAAGGGACGG GCACATCGGC CTCAGCAGGG GCCGCGCCAG GACGCATGGC TGTGACACAC 2460
TTGGGCACCC CTCCGTGTGA GGTCCTGATG GAGGTGCGCC GAGGCTGGGC TGGCCTCCTG 2520
TGCAGGAATA GAGGCCGTTG GGCCTTGTCC CAGCCGGTCA CCTGCTGTTG CGGTCTCAGG 2580
GAGCCAACAC CTCTGAGCCT GTTTGTTCAC CGCTCCCAGG GTAACAACAG GTCCCGCCTC 2640
TGAGTGAGCC GCACTCCACC CCGGTGGTCA CGGCCGGCTC CAGGGCCTGT GAATGGCCTG 2700
TGGCCGCTGC CCTTGGAGGT GACCACTGTG CCCTCTCAGG CTGGCAGGAG AGGCCGTTCC 2760
CTGGGACTTC TCCTACACCC ACAGGGACCC CATGGGATTA GAGCTGAGGT CCGGGGCGGG 2820
GGCAGGTGGT GGAGACCAGG CTCTGGGGTT ACTGTGCCTG GGAGCAGCCT CCTGCTTCAG 2880
GTGCAGGCAC CGGACATGCA GGGTCAGGGG CCCAGCAGGA GCTGCCTGGC CAGGCTTGTC 2940
CTGCAGCTGG GAATGGGGAC CCAGAGAAGG CAATGCCACC CACACCCCCA CCACCGCCTG 3000
GGCCCACCGA GCCTGAGAGG GGAAGGCAGC TCCTCCCCAG GGTGAGCCCC AGGGCCTCGG 3060
GCTGGGGTCC TGCCCCTGTC CAGGCTCAAG GTCCTCTCTC TGCTCCCCTG GTCTCTCCCT 3120
CACCACCCAC CCACCCACCC ACCCACCCAC ACCTCTACTG AGGGCCAAGC ACTCCACTGG 3180
GCCCAGGCTA GAAGGGGGCC AAATGGGGAG GGCTGTGAAT CACCAGTTCC CAAATTAGTG 3240
CATAATCACA CACAGGAACT GCTGAGAAGG AAGGGAAGAG GGGCTTGAAG CAGAGCATCC 3300
AGCGAGAAAC CTGGCCTGGA CTGGGATCCG GGAAGGCTTC CTGGAGGAGG TGGCAGGAGC 3360
CAGGATCTGA ATGGTGAGCT AATCAGGAGC TGATGGGGTG AGGGTGGGGG CAAGTGTTCT 3420
AGGCAGGAGG AGGGCAGGGC ATGTTCCAGG GGTTGCGGAG GTGGTCAGGG GGCCCGGTGG 3480
GCCAAGGCAC AGACTCTGGG TGCTGTTGGA 3510