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

TagContent
EnhancerAtlas ID
HS115-03960 
Organism
Homo sapiens 
Tissue/cell
Kidney_cortex 
Coordinate
chr7:137684450-137686340 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2CMA0497.1chr7:137684580-137684595TTTTTAAAAATAGAA+6.3
ONECUT2MA0756.1chr7:137685991-137686005AAAAAATCAATAGC+6
ONECUT3MA0757.1chr7:137685991-137686005AAAAAATCAATAGC+6.39
ZBTB18MA0698.1chr7:137685141-137685154GAACATCTGGCTT-6.19
ZNF263MA0528.1chr7:137685903-137685924GAGGAAGGGAGGGAGAGAGGG+6.08
ZNF263MA0528.1chr7:137685899-137685920AGAAGAGGAAGGGAGGGAGAG+6.2
ZNF263MA0528.1chr7:137685902-137685923AGAGGAAGGGAGGGAGAGAGG+6.32
ZNF263MA0528.1chr7:137685907-137685928AAGGGAGGGAGAGAGGGAGAG+6.57
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_00066chr7:137682492-137687567Adipose_Nuclei
SE_01161chr7:137684509-137686950Adrenal_Gland
SE_01583chr7:137684403-137685439Aorta
SE_02254chr7:137682808-137687098Astrocytes
SE_06592chr7:137683434-137687395Brain_Hippocampus_Middle
SE_25824chr7:137682399-137687377Duodenum_Smooth_Muscle
SE_27287chr7:137684459-137687125Esophagus
SE_27744chr7:137684115-137688004Fetal_Intestine
SE_28585chr7:137682481-137687914Fetal_Intestine_Large
SE_30032chr7:137683636-137687749Fetal_Muscle
SE_32391chr7:137684472-137687096Gastric
SE_35591chr7:137684336-137686994HepG2
SE_37226chr7:137683064-137687600HSMMtube
SE_38299chr7:137683850-137688187HUVEC
SE_39130chr7:137684026-137686865IMR90
SE_39990chr7:137684101-137687103K562
SE_44418chr7:137682617-137687032NHDF-Ad
SE_44792chr7:137682826-137687008NHLF
SE_45544chr7:137657492-137687859Osteoblasts
SE_46995chr7:137684630-137685403Ovary
SE_50455chr7:137684229-137687209Sigmoid_Colon
SE_51841chr7:137684123-137687119Skeletal_Muscle_Myoblast
SE_52498chr7:137684207-137687164Small_Intestine
SE_55864chr7:137683778-137687183u87
SE_59162chr7:137664421-137694313Ly3
SE_61141chr7:137663463-137694162HBL1
SE_63629chr7:137683728-137687119HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr7137685065137685809
Enhancer Sequence
CCAATACCTC TTTCAACAGT AATTCATATG CACAGTTTGT TGCACTGACT TGCAGCAATG 60
ATGAGCAGCA TTTTACAGGA ATGAGCTGTT CACAACAGAC ATGTACCTAA GTGGAGGACA 120
TAATAAGCAT TTTTTAAAAA TAGAAATAAA AGAAAAATAA TCACACATTC CTGCTTTATC 180
ACAATGACAG AAAAACTGGG CTGTTAATAT CAAAGCAAAT GTAAGGCCTC TACTCCCTGA 240
AAGTGTGCAT AAGGTGTTAG TTAGAGCCAG TCCAAGCAGT TCTTCCCAGA GTGAATGCCA 300
CAGTCACGGG TAGCATCTCG CACCTTTCCC TGTGAACTCA CAAATGCAAG CTACAGGGCC 360
AAAGAACAGC AAGGTAGATG CCTGTGCGTA ATTCATCCCA CCAGCTGAAA GACAACCCCC 420
TAGCTGTGGC ATTGCAGCTG CTGGATGAGA CACTGTCACA GCGAAAGAAT ACTTCAAGAA 480
CAAAAGAGAA GGGCTGCCCC TCTGCATATG GATAAAATGT AGCCTGTCAG TAGAAACTCC 540
TGGAGCACCC ATTCATCAAA AGATATTTGA GGAACAACAT ACTCCAAGTT CTTTACTGAG 600
GACAGGAAGC ACATCTGGTA CCCCAACCTC CGTGCTGCCC ACATAGTGTC CCCATGACAA 660
GCTCAGCAAG CAAAGCCCAG AAGATCACAC TGAACATCTG GCTTTTGCCC CAGCATGAAC 720
TACCACTCCC TCTCAGCCCT GCACTCTGCA TTTTTTTTAA ACAAGCCACT CTCAGCCACC 780
ACAAATACTT CGGTGGGAAT CAGCAGGGAG GCCCTCATTC CTTGTCTCAA AATAACGTCA 840
GCCAGAGTCA AAGGCCAAAG AGGTGGAGCC TGCAGGCCAT TTTGCGAAAG TTTCAAATAT 900
CTTGGTACTG ACCCCATTAA AAAAGCGTGA AGGGGAAGCA GCCAAGCCTC CAGTGGTTTT 960
CTCATTAGTG TCCCCCCTCA CCCCAGCCCC ACCCCCATTA CAAACGTCTG CATGGATAAG 1020
AATCAAACAA AGAGATCTTG CATAAAGTCC TATGATCAGT GCTGGCTATT GAAAACAAAA 1080
TTTCATTTTG CAAACTTAAT ACCAAAAACT TGACATTAAA AACTTTAAAA GAAATGTGCG 1140
TGCTCTGGGA CAGCTTAATC CCCCAAGAGA TCTCTGAGGC ATTAGTATAA GACTGAACAA 1200
GCAACTGGTG AGCTGTCCCA CCTTCCCCAG AGCCTTTCTT AAATATGCAA CTGTCTCAGA 1260
TTTTCCATAC TCCTCTGCTG GTTTTTCCTC CGAAGAGGGA GGAAGGAGAC TTCTTGGTCG 1320
TACAGTTTAA GAAAGCAAAT AAAGCCGCCT TTCTCCCTAA CGTAGAGGAG CCCTTTCAAC 1380
ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACGTGTACTT TTTAAAATAT 1440
AAATATGAAA GAAGAGGAAG GGAGGGAGAG AGGGAGAGAG AATACGAGAC AGATGAAAAG 1500
GAAATGCTAC TTAATCTTGT CCAGTTTTTG AAAACCTCAA AAAAAAATCA ATAGCAAACT 1560
AGGCGGAGGC ATGTTATTCT CAAAACACAC ACTCCCTCTC CCGCATTACA GTACTGTTAA 1620
CAACAGCAAA TGATATTACA GATGGAAAAA GCCTCAGGGA AAAAAGCATG AATTGTTAAA 1680
GGAATACAAA GTGGCATTAC TCTCATGAGA AATGTAAAGG GGCCAGCTGC CCGCCTTCAT 1740
CTGCTCAGAC ATTAAAGTAC ACCTCGCCCA GGACCTCTTG ATTCTGACCA TGCCCTGCCC 1800
CAAACCCTGC CTTCCCGGGT CCCAGGACTC CAGCTGCTCC TCGCGTGACA ACACTTGCCC 1860
GCTTTGAAAG CCCTCCTGCC CCGCCCGCCG 1890