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

TagContent
EnhancerAtlas ID
HS114-00081 
Organism
Homo sapiens 
Tissue/cell
Kidney 
Coordinate
chr10:81164310-81167460 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MafbMA0117.2chr10:81165608-81165620AGTCAGCAGTTT-6.22
Nr5a2MA0505.1chr10:81166562-81166577CATGGCCTTGAGCTC-6.49
PLAG1MA0163.1chr10:81166841-81166855CACCCTAGGGCCCC-6.8
RUNX1MA0002.2chr10:81164875-81164886CTCTGTGGTTT+6.14
ZNF263MA0528.1chr10:81166642-81166663GGAGGAGAAGGAGAAGGGGCT+6.06
ZNF263MA0528.1chr10:81166639-81166660AAGGGAGGAGAAGGAGAAGGG+6.83
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00142chr10:81156094-81174637Adipose_Nuclei
SE_02958chr10:81167143-81168949Bladder
SE_03174chr10:81163487-81169525Brain_Angular_Gyrus
SE_03898chr10:81156436-81180126Brain_Anterior_Caudate
SE_04817chr10:81155585-81181394Brain_Cingulate_Gyrus
SE_05788chr10:81155625-81183288Brain_Hippocampus_Middle
SE_06728chr10:81155621-81180487Brain_Hippocampus_Middle_150
SE_07768chr10:81155492-81179943Brain_Inferior_Temporal_Lobe
SE_25889chr10:81165250-81170574Duodenum_Smooth_Muscle
SE_26856chr10:81160099-81165993Esophagus
SE_26856chr10:81166199-81168320Esophagus
SE_29837chr10:81155827-81168604Fetal_Muscle
SE_31599chr10:81162237-81173861Gastric
SE_41733chr10:81164049-81172648LNCaP
SE_42381chr10:81156675-81172040Lung
SE_44257chr10:81162183-81166445NHDF-Ad
SE_44257chr10:81166680-81169139NHDF-Ad
SE_46651chr10:81164441-81166252Ovary
SE_46651chr10:81166260-81168203Ovary
SE_48154chr10:81155988-81174003Psoas_Muscle
SE_48769chr10:81162212-81167005Right_Atrium
SE_50469chr10:81156766-81170652Sigmoid_Colon
SE_51284chr10:81155573-81168009Skeletal_Muscle
SE_54372chr10:81156767-81168262Spleen
SE_54563chr10:81155913-81172163Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr108116686381167116
Number: 1             
IDChromosomeStartEnd
GH10I079396chr108115593581171755
Enhancer Sequence
TGCTGTTTGC TGATTGCTGG AGGGGACTAT TGAGTTTGAA AACCATTTGT TGTTTCCAGA 60
TCTTGCACAT CCCTCTTTGG GTCCCGTTTG CTCAGCAAGA CCTTTCTTCC GACTGCACCT 120
CTCTCTCCTG CTGCAGTCAC CGCCTGAGTT GGGCCAGGCA GAATCTCCCC AAATACTTAA 180
ATGAAGGCCC ACTTCAGGTT TGGGCCTCAC CGCAGAGCTG AGATGAAACA TGCAAGGCAT 240
TCGGGCCCCT TCCCCTTCTG GCCCCAGCTG ACCTTCCACC CACAGCACTT ACACTCAAAT 300
AAAGAAAAGT CACTCCCTGC AAGTGACATG CTGCCCATCT GTGCCTTTTT CTTGCTGTTC 360
CCTGTACCCA ACACTTCACC AGTGAACAGC CATGTACCCT TCAAGAGCAA GCTCCAGGGG 420
CACCCTGGTC TCCCTGGCCC AGAGAGGGCT AATGCACTGC TCAGGAGCTC ACTCCACTGC 480
TGAGTCCCAG GCTGGCTGGT GTGGAGATAA GAACCCACCC GCCGCCTTGC CCTGGAGAAG 540
GCCCTCTCCC TGAACTTCCA GGGGACTCTG TGGTTTGCAC CACACGCTTA GCTCCAGGAA 600
AGGCGAGAGA CATGATCTTC CCTAGGTCAT GTCCTGCCCT GACCCAACCT CCAGCTTGCC 660
AAACTCAGAG ATTTCACCCG AAATTTAAAC GAAATTCCCC TACTGCCATC TTGTTTCCCA 720
CAAGCCTCTC TGTGTGCTGC GGTCAGGTGC ACCCTCCACA CCTCTCACTT CTATGGTAGC 780
ACTAGGCTCA GGCTGGGGCT CAGAATCCTT TGGCAGCTGG AGGGGACACC AGGAGTGGCA 840
GTGCCTGCAA AGGGTGAGGT GTGAGGTGGA CAGCAGAAGT TAGGGCAGGG TGGAGGTCGC 900
ACAGGTAGGA GGTGGCAATG CCAGGGCTGA TCATGGCGTG GGCTCTGTCC AGTCCCAGGA 960
CGCCTCCTTG GGCAGTGCTG AGCACCCTGG ACGGCTGTCT TGAGCTAGCA GCGCCATTTG 1020
CACAGGGCAG CTGGCCCCTG GCTCTGTGTC TGAAGGCGTC CCTGGCAAGG CCTGGATAGA 1080
CATGGCCGTG ACCAGCCCAG CCTTCCCTGG CTGGAGGGAA GGTGGTGGGT CAAGAGGTGG 1140
AAAGGCCTCA GCCTGGAGTG AGGCTTTGGG TGTGAGGGCC ACAGCCCTGG GAGGAGGGGA 1200
CAGGGGAGCT CAGCTCAAAA TAGTGATGGG GGAAGGGTGT GCAGGGTGGC CAAGTGCCAG 1260
AAAAGAAATC TGATCTGCCC TGGCCAGTGA AATGCTGAAG TCAGCAGTTT GGGGCCACTC 1320
TGGCAGAGGC CTGGGGGCTG AGGCCCCCAC TGCTGCCTGG CAAGAGGCTG TGGGCGTGAC 1380
TTCCAGCCTC GCAAAACCCT CACATAAATC ACCTCCTCTC TCTGGGATTC GATCTCCTCA 1440
TCTGGGTAGA AAGAGAAGCA AACTTTCCAT CTCTGGGTGA GCGCTGGAGC TCACAGCACT 1500
TAGGAGACTG TGGCAACCAC AGACCGGGGT GGAGAGTGCT GAGTCTCCCC TGCGTGCTGG 1560
GGCTGGCCAC GCACACAACC TGTAGGTAGC TTCATTGTGA TCCCATTTCC AGGTGAGGAA 1620
ATAGAGGCTC AGAGAGGTTA AGTCACCTGT CCAAGGTCAC AAAGCAAATA AGCAGAAGGC 1680
TTCGAACCAT GGCCTTTCTC CCTGTTGCCC AATTCCCTCC TTGCTGAGCG AGATATCGGA 1740
GGTCCAGAAG GCCATGGACA GGTACAAAGG ACACCTGTGG CACCTGTTCT TCAATTGGGT 1800
GGAGGGGAGC TCTGCAGAGG AAGAGCTGCT CTTATGTGAC TTTTACAGGG GGGTCGCAGG 1860
GAGGAAGGAA GCCTCACATT TCCCACCCCT GCTGACCCTG CTTCTTCACC AAGGGGCTGG 1920
AAAGACATTC CCAAACTGAC CTTTCTCCAC TGTCCCCAAA GGCGAGGGTG TTCTGTGCAG 1980
GAAGCTCTGC AGGAAGCAGG ATGATGGAGT GTCCCCAAAT GGTCACTTCC CCTGCCTGGG 2040
CCCCAGGTTC CCTGGCTCTA AAACCCTCAC AGCTCCTGCT ATGTGTGGGG TTACCTCCAC 2100
CAGCCATTTC ATCCTCCCTG TAACCCCTAC AGATGAGGAA TCCAAGTCAC AGAGAGGTTA 2160
AGAGATTTGC CTGAGGTCAC ACAGGCAGGA AACAGCAGAG CTGGGATCTG AACCCAGGCC 2220
TGACTGACTG CTGCAACGCC GCATGCCTCC TACATGGCCT TGAGCTCTGA CCTCCTTGCC 2280
CTTGTCTGTG GACAGCCCCA CAGGACAATA ATCCCGCTGG TGCCCTGAAA AGGGAGGAGA 2340
AGGAGAAGGG GCTGGCTGGT GGTACTTGTT TTCATACCCA CCTTTACACA CCCCAGTCTC 2400
ACTACCTGGC ACACCCTGCC TCCCAACCAA ATCCAGTGGA AGCTGCACTT CCTCCGGGAA 2460
GCCTCCTTGA CCCTTCTGGT CTCTGTCCCC TTGCCCCAGG GCTCCTCTTG TCACTCTCTG 2520
TGCCACAGTG CCACCCTAGG GCCCCCTCTA CACCTGCTGA AGGCAAGCTG GACACACGCC 2580
CCGCAACCTG TGTGCACACA TGGCCTCTTT GCTAGGGTCT GAGACAGCGC CTTTAAAGTG 2640
CTGATGGGGT GGAGCGCCAG CCAGGTGCAG ACCTGCCCCC AGGGAGCGCC TGTCCCAGAG 2700
GAGCACTCGG TGGTGTGGGA GCCAGGCTGA CTGTTGCACA GTAACCATGC CACACACAGG 2760
GCTGGGAGCG CCAGTCCACA TTCCCCAGCA GGAAGTGAAG GCTCATTCTG AAGCCATACG 2820
GCTGTGCTCG TCTTTCTGAT TCCAGATTCC TGAGCCCCTG CTTCTAGAGC ACACGCTCTT 2880
CTTCGCTCAC GAGAGCACGC ACAGGACCAT CGGGGCATTG GTACACTGCA CGCTGCTGCC 2940
CTGGCCCCAG AGTCTCAGAA TCAATAGGTC TGGGGAGGGC CTGAGAACCA GAGTCTCAAA 3000
TGCCTGGGCG GTGCAGCTGC TGCTGGTCTG GGGACCCACC TAGGGAGCCA CCGCCCCAGT 3060
GATCCTGGTC ACAGTCTGTT AAAGTCCAGT CAGATACTGT CACCTCCATG CTGTCCCCAT 3120
CTGCCCATTC TACAGCCCAG GAAACTGAGG 3150