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

TagContent
EnhancerAtlas ID
HS187-22263 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr7:1570650-1573760 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr7:1570894-1570905GGGGGCGGGGC-6.02
KLF5MA0599.1chr7:1570720-1570730GCCCCGCCCC+6.02
KLF5MA0599.1chr7:1570895-1570905GGGGCGGGGC-6.02
KLF5MA0599.1chr7:1570900-1570910GGGGCGGGGC-6.02
MAXMA0058.3chr7:1573120-1573130ACCACGTGCT+6.02
RREB1MA0073.1chr7:1573214-1573234CCTGTGGGGCTGTGTGGGGG-6.1
Rhox11MA0629.1chr7:1572275-1572292AGGCTGCTGTTAAGGGA+6.46
SP3MA0746.2chr7:1570893-1570906GGGGGGCGGGGCG-6.11
ZNF263MA0528.1chr7:1573373-1573394GGATGAGGAAAAGAGAGAGGG+6.74
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01055chr7:1570046-1578500Adrenal_Gland
SE_01774chr7:1570429-1574731Aorta
SE_02367chr7:1570330-1574348Astrocytes
SE_03104chr7:1570503-1573715Bladder
SE_23223chr7:1569889-1574340Colon_Crypt_1
SE_23806chr7:1570006-1574230Colon_Crypt_2
SE_24753chr7:1569977-1574461Colon_Crypt_3
SE_27330chr7:1569886-1575089Esophagus
SE_31493chr7:1569977-1575137Gastric
SE_34826chr7:1569156-1574822HeLa
SE_38079chr7:1569712-1579680HUVEC
SE_40839chr7:1569746-1579732Left_Ventricle
SE_42397chr7:1569896-1580027Lung
SE_44885chr7:1570653-1574696NHLF
SE_47487chr7:1570011-1574531Pancreas
SE_48363chr7:1569732-1579166Psoas_Muscle
SE_48876chr7:1570285-1575118Right_Atrium
SE_49556chr7:1570289-1574659Right_Ventricle
SE_50439chr7:1570130-1574512Sigmoid_Colon
SE_51421chr7:1570586-1579607Skeletal_Muscle
SE_52714chr7:1569796-1574595Small_Intestine
SE_57087chr7:1570309-1572594VACO_400
SE_57087chr7:1572656-1574376VACO_400
SE_57731chr7:1570257-1573660VACO_503
SE_58039chr7:1570315-1572628VACO_9m
SE_58039chr7:1572686-1573505VACO_9m
SE_65442chr7:1570666-1575028Pancreatic_islets
SE_69146chr7:1572601-1574189H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 7             
ChromosomeStartEnd
chr715708031571011
chr715718001573183
chr715712731571500
chr715722621572844
chr715735241573718
chr715712351571800
chr715718481572026
Enhancer Sequence
CGGGGTTGGG TGCGCGGGGC CCGAGACCCT CATGCGGCCC GCGGCGCGGC CCGGGCACCT 60
GCCCAGGTGG GCCCCGCCCC GCAGGCCCGG GGGCTTCCCC GGGACGCGAG GCTCTCTCCC 120
CTGCACGTGC CGCCCGGGCC ATGCTTGCCG CGCCGGGGGC CCCAGGGCGC GGACCCCAGA 180
CCTGGGAGGA CGAGGATCCA CGCGGGTCGG CGGCGCGCAT CGGGCCCGCG CCTTCACACC 240
TGCGGGGGGC GGGGCGGGGC GGGCGCCACG TGCGGGCGGT GCGGGGAGGG CGCGGGCGCG 300
TGGATTCTCC GCGGCTTCCG CCCCAGCGTG GCTTCCGCGT GCGGCCCCGG ACTGCCCCCC 360
GCGCTTCCTC CCGGTGACGG GCGGCGCTCT GGCCCAGTGG CTGGGGTCAC GCGTGCCCGG 420
GAACGGGGTG GGGGTAACCG GGTCTCCCCA CAGGCGGGAT CCTGGGACTG GTGTCGCTCT 480
CAGCCGCCCA CCTGCCAGGG TTGCTGGAAG GAAGGCCGTG GGGAGGCGGG AGGGGGGCAG 540
GTGACAGTGG CCCCAAGGCT CGTCCCTTTG CTCACGTGTG GGGCAGGGGC TCCGGCCTCT 600
TCCCGCTCCC ACTGCGTGAG TTCTTCTGTG CCTCTGTCAA GTTCAGGAAA CTGTGTATGT 660
GCCCGTGACT GTGTGTGTCT GCGTCTGCAC AGCCTCTAGA TCCTGGGGGG TGGGACCAGG 720
CGCCACCGAG AAACCCAGAA AGCCAGGACC CCGCCTGGCC TTGGCCCTTG ACCTGGGTCC 780
GCCTGGGACA CAGCAGTGGC CCTGCACTGC ATTCTCGCGC TCACACCGTG TGTGTCCGTG 840
TTCGCGGGGC CTCCCGTGTC CCTCTCCTGG TGTCCTGCGT CCCTGAGCAT GCTGTTTTCT 900
TGCTTCTTAA GTAGCTCTTG TAGCTGAGGC AGAAATTAGA TCCACTCACC ATTCATTCAC 960
CAGGTGACCC ACAGGCAGCC AGCCAATCTC TGGCCAGGTG CCTGGCCTTG GGAAGATCCT 1020
GAGACTCAAA ACGCCCCCCA CCGCCCCCCA TCGTGGTCTA GGGGATATCT GTGTGGTTCG 1080
GCTCTGGCAG CGCCCTTCCC ACCCCTCTGA TTCTCCAGGG TGGGCTGCCA GGTCTCTTTA 1140
CTGGCACTGA GGTTTCACCG TCACGGTGTG TTGTTGTAAG GGGTTCTCCA ACACAGAGTG 1200
GGGTGCCCTA TGCAGCTTCT CCAAACCCAA TGTCTTCAGG GACATGGAGC ATTAAAAGAG 1260
CCGTGGGCGG GGTCTGGAGA ACATAGGTGG GCTGTGCAGG TGTCTGGGAC ACACCTACAC 1320
CCTATTTGGG CGTCCAGTGC CATTTATGAG AACATCTCCC TTTCTTAGGT AACCCAGTAG 1380
GAATGTCTGA GTTTGACCTT GGGAGAGGGA GTCTGCTTTT AAAACTAGAC CTCTCATTAT 1440
TCCAAAATAA GACATTTATT AAAGCAGAAA AACCAGGCTT CTCCTGCCTT TTATCCTTGA 1500
ACCGAGCCAG GGCTTTGAGG GGCTGGTTGC CCGCAGCGTC GACTCCCCAG GTGCTGGTAA 1560
ACCCGGGAGC CAGCGTTTAC CGAGGGTCAG GGTTGTCGGG GCGCCAGCCT TTGTGTGCAC 1620
CCGGGAGGCT GCTGTTAAGG GAGACCGTCT TCCGGGCCAC TTCGCTGTCT ACAAGGCGTG 1680
TGCTTTCACC CACGGGGCTC AGCGATGGCT GCGTTTGTTT ACAGTCTCTG GCAAAGCTGT 1740
TTGCCACCCA GACGGAGAAG AAGTTGTGCC TGTTCTTGTC CCAGCTGTTT CTGAGTCTAA 1800
AGGTTTCTGG AGTGGACTTT CTGGGTTTCG GGTCCAGTCC ACACGGGAAA TGGAAATCTG 1860
GCCAGCTGAG AGAGGGCTCC GTGTGGCCGC CTTTCAACAG TAAACAGTGA CTCACCGCTC 1920
CGTCCCCACC CTCCCTGCTC TCCGCGAATG GAAGATGCCT TTCCCCGCTA TTTATTTTTG 1980
CTTTTTATAA GTCACAGACT CGTCATGTTT CCGCTTTCCT ACAGTTTCAG GAAACTGGGA 2040
GTGTCGTCTT AAAATCATAG AGTTTTAGAG CAGGTACAAG CGAACTTGAG TGGCCACATG 2100
CCCCACCCCC CGACCAGCTG CTGTAGATGA GGAAGCCCAG GCCATGAGGT CTGCTGGCCT 2160
GTCCCACAGG CCGGTGGGGT CTGGTGTAGA GCCTTCCTGC TTCTCCGCAC TGTGCGTCGG 2220
GTGTCCTGGG GAAGGTATTG GGGTGGAGAC TGCCCTCTCC CTGCCCTCCC ATGCGGGGCC 2280
GGCTCATCTC GTACAGCGGG GGCTAGTGTG GGGTGTAGGG AAGACCTTCT CCCTGCTTGC 2340
AAGGAGCTCA CCATGCCTTG GGGAGGCCCC CTGTCCCCAG AAGGATCTAG AACCAGGCCT 2400
TGGTAGAGGG TGCTTGCCTA CGCGAGGAGG AGAGCAGTGG GGAGTGTTTC TGGAAGAAGC 2460
AGGGCAGGGA ACCACGTGCT CTCTGCAGAT GGTGATCAGA AACCTGAAAC GGCATTGGGG 2520
TGGGGGAGTC GGGGTTTGGG AGGAACCCCC AAGACTTTTG ACTGCCTGTG GGGCTGTGTG 2580
GGGGGCACCA GGATCAGGGT GAGGGCATCC CATTTGGCAA AGCTGTGGTC CAGACAGGAG 2640
ACGCTGGAGG CCGGAGCCTG GGCAGGTGCT GTGGGTTCAG GCGGGTGATG CTTGAGGGCT 2700
GGGATCAAGC CTGGTTGGCG CGTGGATGAG GAAAAGAGAG AGGGGCAGGG GCAACTCCGG 2760
TGAATGATGC GGTTGGGGGC TGGGGGGCAT CTGGGCCCCC CGGAATGCCC CTGACTGGAC 2820
TTAGAGGCTG GGAGCGGATT GAAGCCCCAG GGCGGCCGGG GGAGAACAGG ATGCTGATGG 2880
GGAGCTGGAG GCCGAGGACA GGAGGATGGT GTGGTGGGAG CCAGGGCGGG GACTGGAGGG 2940
GGTGTGGTGT GTTCTGCAGT CTGCTCTCTG CTGCTGCAGC TGCCTGAGTC ACCTCTGGAT 3000
GTAGCGGAAT GACACAGCTT CCTCAGACTG CAAATGCAAG GTGACCAGAC GTCCTCCAAG 3060
CCGGGCCGAC AGTCATGGCT TGCTGGAGGG CAGCCAGCCA GGGCCAGGCT 3110