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

TagContent
EnhancerAtlas ID
HS115-00125 
Organism
Homo sapiens 
Tissue/cell
Kidney_cortex 
Coordinate
chr1:33218990-33221990 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr1:33221585-33221596GAAGATAAGAA-6.02
KLF16MA0741.1chr1:33219795-33219806GGGGGCGGGGC-6.02
KLF16MA0741.1chr1:33219551-33219562GGGGGCGTGGT-6.14
KLF5MA0599.1chr1:33219498-33219508GCCCCGCCCC+6.02
KLF5MA0599.1chr1:33219796-33219806GGGGCGGGGC-6.02
SP1MA0079.4chr1:33219495-33219510CAGGCCCCGCCCCTC+6.22
SP4MA0685.1chr1:33219495-33219512CAGGCCCCGCCCCTCCT+6.32
ZNF263MA0528.1chr1:33220523-33220544TCCCCCCCTCCCCCGTCCCCA-6.03
ZNF263MA0528.1chr1:33220656-33220677TGGGGAGGGGAGGGAAAGGGG+6.2
ZNF263MA0528.1chr1:33221575-33221596GGAGGAGAGAGAAGATAAGAA+6.32
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_00938chr1:33219006-33222393Adrenal_Gland
SE_23116chr1:33219622-33222368Colon_Crypt_1
SE_23802chr1:33219124-33219553Colon_Crypt_2
SE_23802chr1:33219604-33220504Colon_Crypt_2
SE_23802chr1:33220519-33221309Colon_Crypt_2
SE_23802chr1:33221322-33221788Colon_Crypt_2
SE_24863chr1:33219103-33221902Colon_Crypt_3
SE_26629chr1:33219003-33222323Esophagus
SE_28121chr1:33220540-33221955Fetal_Intestine
SE_29204chr1:33219822-33221616Fetal_Intestine_Large
SE_31442chr1:33219069-33222394Gastric
SE_32998chr1:33219539-33221354H1
SE_34017chr1:33218987-33219471HCC1954
SE_34017chr1:33219830-33221722HCC1954
SE_36587chr1:33219820-33221157HMEC
SE_41588chr1:33219113-33221709LNCaP
SE_47530chr1:33219105-33219467Pancreas
SE_47530chr1:33219506-33221824Pancreas
SE_50335chr1:33220528-33222187Sigmoid_Colon
SE_52480chr1:33219537-33222050Small_Intestine
SE_64801chr1:33219051-33219585NHEK
SE_64801chr1:33219594-33221668NHEK
SE_65538chr1:33218762-33221927Pancreatic_islets
SE_68878chr1:33219160-33221410H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr13322118433221695
chr13321948933220800
chr13322098733221800
Enhancer Sequence
CAGGAGAATC GTTTGAACCG GGCAGGTGGA GGTTGCAGTG AGCCGAGAGC GTGCCCCTGC 60
CCTCCAGCCT GGGTGACAGC GAGACTTGGT CTCAAAAAAA TAAAAAAAAT AATAAAAAAA 120
GGACCTACCT TACACAATTG TGGATAAAAT GAAGTAATGC ATGAAAGCGG TTAGCACAGA 180
GCCTGGCACA TAGTAAACAC TAAGTAAAAG GGTGCTACTA TTTTGAACAC TGTAACTACA 240
GAAATACAGT CAGTTCGATA CATTTGTACA CACAGGCACG TGACAGTCAC GGGGAGGTGG 300
CTGGTGGGCT CTAGCGGCAG CAGGGCTGCG GATCCGCGTT CTCCCAGCTC CATTGCACTC 360
CTCAGAGCGG TAGCCTCTGG GCTGAGAGAG TGGGCAACCC GCCTGCCCCA CCTGGACTGG 420
CCAGGCCTTC CCCTGTGCGC CCTAGGCTGG GCGGCTCAGC CGGTCTCCCA GGTCCCGGGA 480
GGGGCGGAGC CGACGGGATG CGCGCCAGGC CCCGCCCCTC CTCCGGGCCC GCCCCCGGCC 540
TGGCCATTGG CCGCAGAGCT CGGGGGCGTG GTCGAGCTGG GGCTGGGGGC GCCCGCGGTG 600
CCCGCCCGCG AGTCTCGCTG CCTCCCTCCC GGGGCTGCGG GCCCGGCGGC CGGGCTGGCT 660
GGGCCGCGCT TGGGTTCCCG CGCCGGCTCC CGCACCCGCA ATGGGGAACT CACACCACAA 720
GAGGAAGGCC CCCAGCGGTC CCCGGGTCCG CAGCTTCTGG CGGTTCGGGC GGTCGGCGAA 780
GCGGCCGGCA GGTAGGGGCC GGGGTGGGGG CGGGGCAGGC AGGGAGGAGG GTCCCTACTG 840
CGGTCGTCGC CACCGCTGCT GCCCCCTCCC GGGGCTTGGA GGGTGTGAGT GTGGGGGGGT 900
CGGGAATCCC CGCGCAGACC CCACCCCTCA CAGGCACACG GAGACACACG TACACGGTAA 960
TACCTACGGG CGGGCACACG TACATGTTCG CAGTTTACAC AGTCACACGC ACAACACCCA 1020
CTCAAATGTA CGGACACGCA GACACAGGAT CACATACACC ATCACACCCA CACTCTCGTA 1080
CCATCGCAGT AGGACGCACA CAGCCTGAGA CATAGGTACA TGTATACCTA TGCATGCGGT 1140
TTACACAGCC ACACGAACTA CACCCACGCG CAGATCCAGA CACACAGGCA CACAGTCGTT 1200
CACACACATC GGTCATGTGG GTACAGTTGC CCAGCGTCTT AGGCACACAG ATGTACACAC 1260
AGGTTCATAA CTGCACAACC AACCGGACTC GCATTCAGGC TCACAGCAGA CCCTAAGGCA 1320
CTCGGACACA CACGCTTATT TCCCAGATCT TAGCCCCCAA CAGGCTGAAG GCTGAAAGTT 1380
TGTAGGAGGG AGGGGAGACA AAGGTGGAAG GGAGAAGCTG GAAACCCGGG GCTGGAGTCT 1440
GGGGACCGCC TCCATCTGGC GCGATCGGGA GTCGGACTGG TTTTCTTGGC TCCCTCCCTA 1500
CCCCCACCCG CGCCACCGCG ACTTCTCCCC GCCTCCCCCC CTCCCCCGTC CCCACGGTCC 1560
CCGAGGTCGC CGCCGCATCT CCCCCTTTCA ATGCAGCCAC CGAGCTGGAA CGCAGCCCTT 1620
GCCGGCTGCT GCGGGATCCC TCCGCGGGTC ACATTCCAGG CTCCAATGGG GAGGGGAGGG 1680
AAAGGGGAAG GCCTCCAATC CCAAGAGATG GGATTCCTGT TTCCCCCAAC AAGTGCGGCA 1740
GTTCAGGGTA TCCCCGAGGG GCGCTGAAGG AGGGGCTATC GAGAGTGCCT AGTTACTGGT 1800
GAATCCAGAG ATGGGGGAAG GGCAGGGTGA TGGTACCATT CCCTCCTCCC CAAGATAGAG 1860
GGTCTTCAAC ATAGGCAGGC ACTTTAGCGA TACCTGTTGG TCTGGGGGAG TGAGGAAATC 1920
CCAGAGGAGG TGGAGTGAAG GGGGCCCTGC TGTGGTGGGA GAATCTACGG GTGTATTCCC 1980
AGGATGGCCC ACATTCCTAG AGATTCCGAA CCGGAGCTTG ATGATCTCAT CGCTCCATGG 2040
AGGGGGTGGT GGAAAGAGCC TGGGCTGGGA AGTGGGGGAC CTCTCCTCTC AATGAGGCTG 2100
TGGAATAGGC CCTGGTGACC TTGAGCAGAT TCCTTTCACT TGTCTGGACC ACTCTGGCTC 2160
CTACAGGGGT TCTGTCTGTG AAATCAGGGG CCCTAGGTGA CTTCTTGGGA CACTTACTGT 2220
TCTGGCTAGC CATTTCATGG ATGACGAGAC TGAGGTCCAG GAAAGAGGGA CTTGTCCAAG 2280
GTCATTTGCC TGTGGTGGTT TGAGGTAGTA ATATAATCAA AATGACAATA AGAAAAGGGT 2340
TAACTAAGTT CAGTTAGGCT CTTTGAGGAT TTCTCAGAAG GTAGGTGTTG ATGAGAATCT 2400
CCAGGACCTT CCAGCACTCT CCCTGCCCCA GCAGTCCTGA AAGCCCTGTC TGTGCCTACC 2460
TGTCTCTCCT AGAATCTGCA CTAAGGGGGC AGGGCTGGGG CTCTTCATCT GTCCTCTGAT 2520
GGTCGCTCGG ATCTGATGGT TTCCTAGGAA CTAACTGTGG GCCCAGACTT GTGACCATTT 2580
GTGATGGAGG AGAGAGAAGA TAAGAAGGCT GTGTTTATAG TCTCTTGCCT ACTGGCCCTT 2640
GAGGAAGTGG CCTGGGGCTT CCAGCAACAC TTGTGAGCTT CCAGTTCCTG CTGCAACTTA 2700
TGGGTCAACT CAAGCTTTAA GGCGTTCTGA AAAAAATTAG AAAGCAATGT CAAGACAACA 2760
CAGAAATTAA GTGTGAGGGG CTAGGAAATA TTCTAGGCAA TATATCAAAA GCCTTCTGGG 2820
TTGGGGTCAG CTTTAGAAAA CTGAGGAGAT GGTCCTAATT TGTCTTTGAA GTAATCACAG 2880
GATTGAAATT AGTCCTAAAT TGTTGGTTAA ATGAGAGAAC CAGGGATTTG TTTCAGCTGT 2940
GGGGTATGGC CGTGAGTAAA GGCATGGAGT TGAGGTCAGG CGAGGTGGTT TATGCCTGTA 3000