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

TagContent
EnhancerAtlas ID
HS115-00033 
Organism
Homo sapiens 
Tissue/cell
Kidney_cortex 
Coordinate
chr1:8476850-8479700 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs115109046chr18477866hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXA1MA0148.4chr1:8477190-8477206AATTGTTTATTTAAGG-6.15
Foxq1MA0040.1chr1:8477190-8477201AATTGTTTATT+6.02
Pou2f3MA0627.1chr1:8477353-8477369GTCTATGCAAATGACA+6.09
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00045chr1:8465614-8485937Adipose_Nuclei
SE_02022chr1:8477510-8478261Aorta
SE_03407chr1:8479298-8480064Brain_Angular_Gyrus
SE_04978chr1:8478743-8481068Brain_Cingulate_Gyrus
SE_06073chr1:8479138-8485793Brain_Hippocampus_Middle
SE_07042chr1:8478805-8485534Brain_Hippocampus_Middle_150
SE_07921chr1:8477474-8483841Brain_Inferior_Temporal_Lobe
SE_11329chr1:8474464-8493359CD20
SE_18764chr1:8477368-8486022CD4p_CD25-_Il17-_PMAstim_Th
SE_23717chr1:8479176-8479684Colon_Crypt_1
SE_25808chr1:8476636-8485754Duodenum_Smooth_Muscle
SE_27457chr1:8477725-8478732Esophagus
SE_28078chr1:8478132-8486070Fetal_Intestine
SE_29095chr1:8478033-8485919Fetal_Intestine_Large
SE_31622chr1:8477645-8478284Gastric
SE_31622chr1:8479255-8479634Gastric
SE_40658chr1:8476604-8477230Left_Ventricle
SE_40658chr1:8477420-8481421Left_Ventricle
SE_41679chr1:8477672-8478706LNCaP
SE_42166chr1:8477479-8478781Lung
SE_42166chr1:8478827-8481118Lung
SE_45677chr1:8477327-8485510Osteoblasts
SE_47251chr1:8465934-8485673Panc1
SE_48103chr1:8477498-8481110Psoas_Muscle
SE_48600chr1:8477483-8479198Right_Atrium
SE_48600chr1:8479269-8481116Right_Atrium
SE_50481chr1:8479223-8481104Sigmoid_Colon
SE_51176chr1:8473915-8486131Skeletal_Muscle
SE_52725chr1:8477578-8478762Small_Intestine
SE_52725chr1:8479134-8481145Small_Intestine
SE_53408chr1:8477393-8478777Spleen
SE_54752chr1:8475052-8485774Stomach_Smooth_Muscle
SE_58576chr1:8455425-8501956Ly1
SE_60758chr1:8454848-8500160DHL6
SE_62661chr1:8450826-8509851Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr184776378478703
Number: 2             
IDChromosomeStartEnd
GH01I008416chr184766058477230
GH01I008417chr184773948478781
Enhancer Sequence
CAAGTCTGCA TTACTGTAAA TAGCGGTGCT TCCTAAACTT TACAGTACTT TGGAATCCTC 60
TGGGGGGTCC GTTAAAATGC AGATTCTGGC TCAAGAGACA AGGACAGGGC CTGAGAATCT 120
TCCATTTTAA CCAGTGATGA GAGTGCTGGC CTGAGGAGCA CACTGTGAGC AGTGAGGATA 180
GACAACGTTT GTAGAAGAGG GACAAGGTTT AAAAACAGAG ATCTTCTAAT GTACTGGTAT 240
GTGGCCGTGA CACATTTGCA CATTCTCAGT AGCATCAACC GACTAAGGAA GTCCATACTT 300
TGTTATGCAA CATTAGATTA AGCATTAATG AGGCTAGGAA AATTGTTTAT TTAAGGTTAT 360
AACCTGAAAT TAAATAAAAC TTCAGGCTGG AAGCTCATAT TGAATACTAG AATCATTTTT 420
AACCTCTTAA TATTAACAGA AACCTGATTA CTCAGTCTTA AAGCCCTTTC TCAATAGCAT 480
TTATTCTCTG CTGCAGGAAT ATGGTCTATG CAAATGACAT TTTGCCTGAA GAAAAAAGTA 540
CAGTTAATGG CCAGTAGTTA CGTACGTATT TAATAGAATT CATTCCCAGA AATGTGGCTA 600
AGAAAGGTGG TTGATTTTCA TGTTATTTAT TAAATTAAAA ATTTAAATCT CTAATACCTT 660
TCATCCCATT ACTTAAAGTT AAAAACGTCA AAACTGGCTG CCCTTTCACT GGGCCCTTGG 720
TGCCAAACAG TGACACATTT CCAATAGAGA AAATGAAGAT AGAAGGCAGG CTTCCCTTCC 780
CATTAACTTT GAACTTTCAA GTCCCTATCT GTCTTCCTAC AAGACTAAAT TATAAGAAGA 840
GCCTCCTCTT TGGTCCCATC CTATACATAC TTCGGTAGCA CAGCCCTCAC TTCTCTTCTT 900
AAAAGCCTTA AATGGGTCCC ATCCCCACAC TCACCCATAC ACATTCTTTG GAGGGAATTC 960
AAGGTCCCCC AAAATCTACC CTGCAGCTAT AATTTGGGCC CAAGTTCTAC TGCATCCGCT 1020
TATGCAACCT CCTTTCCAAC CATGCTCATG TACTTGCTGG GCACGTTTTA CAATTTCCTG 1080
TCTCCGTGCC TTTGTTCATA GTATTTCCTA TGGCTGGAAA GTTGCTTTTC CTCTACCCTC 1140
CCAACCTGGG CCTGTCAAAA ATGAATCCTT CCTTCAAAGC CCAGTTCAAA CACCGCCCCT 1200
CCAATTAGCT TTCCAGGAGC CTCTGTGCTC ACTTTGTGGG GCCTGAACCT CCACCCACCA 1260
GGGCCCTCAG CACATTCTAC CAAGTATGGC AGGTATGTAA ATGTCGTGCT GGCTCCCTGC 1320
AGGGCAGGGA TGGCACCTTG CTTCTCTTTA TAGATACCCT ACCCATTGCA GTGCTCAGTG 1380
GGCACCCAGA ACTTTAAAAA ATTGAACTAT ACACAAAATT TAGTTCTGAT AATGGGAAGT 1440
GAATGAAAAT GAGTTTCCAG TGTAGTAAGT GTCAATGCAC CACCAACTGG GATTACAAAT 1500
GACACAAGCT TAATCTTCAC TGGGCTAGGT GCTCAAAAAT AAAAAGAAAG AGACGAGAAA 1560
GACAGCCAAA GCATGTCCCC TTTCACCTTC CATCTCCCTC CAGGGGCTAA CACTTTGGGA 1620
ACACCTCTTG GCTACCAAGC TGGGGTAGAT CACATTGTCT TCTCACCAAT CTTAGTTGCA 1680
CCAGAGACAA GCAACGGCAG GTCACTGAGG AAGCGCTCCT GGACTACGAC CCAGTGCCAG 1740
CTGAATTTGT CTAAGTAATA GGAGACACAG CTATAAACAA AGGCCAGGAT TCAAGGGACA 1800
ATCATCCAGG TGCCAGACAC AAAAAGTCTT TGGTTCAAAT AACTGATATG TCCTCAGAGA 1860
AGAGATATGT CACCACTGCT TGAATAATTA TCTCATGATT TTGAAGAAAA CTGCAATGTA 1920
TAGACAAATC AAACAAAAAA TTATTTTTGG ATCATCCACG ATTTTGTGTT ATTCCTAACA 1980
TGGATTCACC TTTAGGTAAT TAAGATTCTC TATTAGGCCT CCTACTTTTT CAGGCATTAC 2040
CTTAACATCA AAGCTCATGT ACCATCCATC TACCCAACAA TAAGTGGCAG GGCTCAAAGC 2100
AGAATCAAGA GGCCTAGTTC TCCACTGTCC TCCCAAAAGT TCAGACACCG GGCGCTCTGT 2160
GACTTATACA AATATACTAA CACTTAAGAC TCTGATGTGG TTTATGACAA ACAGTGGCTT 2220
GACAGAGAAG AGGTATACAG CCAAGGTGAA TCTAAAATGC TCCACCCGTA TTCCTGACTA 2280
CATTTCACCT ACTAATTATA TACTTTATAA GCATATTGAG GGGAGGTAAA TGGTTATAGA 2340
GAAACAGAGA ATGGGAAAAA GTATAATAAA CTACAGGATA TTTGCACAAC CATGACACTA 2400
AAAGATTTGA CTTGTAGTTA TTCTCTTGGG TACCCTGAGG TTAACACGTA ATACCCATTC 2460
AACTAAGCCT CTATAAACAG TTGGGTTTTC CGCAATCACA GCCACTATTC CCACTTCAGT 2520
GGGCAGCAGT GTTCAGAGAA AAGCCAGATT TAGCTCTTGT GCAATAAACA CCAGAAACCA 2580
AAAGAGCTAG GAAAGCTGTT TACGTCTATG CCCACCAGGA ACCCTTCTCT GCTATAACCG 2640
CATGAATGAA CTGGTAAGAA TGAGGTCTCA ACAAAGCTTC AAGACGGACG TTGTTAACTA 2700
GTTGCTGCCC TCCAAGTTTT TGGCAAGACA GATTAATGAA AAACAGGTAA CTTATTTTTA 2760
TACAGGCTCA GTATATTTAC AAGCAGAAAG GAATTCTGTA CTTTTCAAAG CATTTAGCTA 2820
CCACCTTATG TAGTATTTAA GGTAGACAGG 2850