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

TagContent
EnhancerAtlas ID
HS051-08385 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr14:77421710-77424710 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr14:77424056-77424074GGAAGTCAGGAAGGAAAT+6.28
MAFFMA0495.3chr14:77423113-77423128CTGCTGACTCAGCAC+7.55
MAFFMA0495.3chr14:77423113-77423128CTGCTGACTCAGCAC-7.61
MAFGMA0659.1chr14:77423110-77423131CCGCTGCTGACTCAGCACTTC+6.16
MAFGMA0659.1chr14:77423110-77423131CCGCTGCTGACTCAGCACTTC-6.47
MAFKMA0496.2chr14:77423111-77423130CGCTGCTGACTCAGCACTT+6.78
MAFKMA0496.2chr14:77423111-77423130CGCTGCTGACTCAGCACTT-7.17
ZNF263MA0528.1chr14:77422786-77422807ACCCCCTCCTCTTGCTCCCCT-6.14
ZNF263MA0528.1chr14:77423475-77423496CCCTCAGCCCCAGCCTCCTCC-6.19
ZNF263MA0528.1chr14:77423459-77423480TCCCCCCCACCCCCCTCCCTC-7.47
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_01254chr14:77420883-77424353Adrenal_Gland
SE_08284chr14:77420765-77424468Brain_Inferior_Temporal_Lobe
SE_24529chr14:77421777-77422089Colon_Crypt_2
SE_24529chr14:77422128-77423800Colon_Crypt_2
SE_24529chr14:77423804-77424327Colon_Crypt_2
SE_27091chr14:77419455-77426235Esophagus
SE_29618chr14:77420671-77424362Fetal_Muscle
SE_31928chr14:77421729-77426154Gastric
SE_32994chr14:77421752-77424066H1
SE_33446chr14:77420480-77424488H2171
SE_34422chr14:77418557-77429646HCT-116
SE_34742chr14:77415823-77429622HeLa
SE_37233chr14:77415973-77429404HSMMtube
SE_38430chr14:77419198-77429214HUVEC
SE_41258chr14:77419224-77429300Left_Ventricle
SE_41987chr14:77421767-77424998LNCaP
SE_42676chr14:77420714-77426260Lung
SE_44184chr14:77419413-77424284NHDF-Ad
SE_46080chr14:77419415-77424550Osteoblasts
SE_46723chr14:77422105-77423789Ovary
SE_47949chr14:77422035-77423590Pancreas
SE_48706chr14:77421709-77426250Right_Atrium
SE_49653chr14:77421766-77424358Right_Ventricle
SE_50880chr14:77420706-77424364Sigmoid_Colon
SE_53991chr14:77419420-77424483Spleen
SE_55769chr14:77419401-77424613u87
SE_65382chr14:77419164-77426315Pancreatic_islets
SE_67544chr14:77419401-77424613u87
SE_68739chr14:77421020-77425262H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr147742376377424258
chr147742224077422571
Enhancer Sequence
ATTACAGGCG CCCGCCACCA CGCCTGGCTA AATTTTGTAT TTTTAGTAGA GACGAGGTTT 60
CACCATGTTG GCCAGGCTGG TCTCGAACTC CTGACCTAAG GTGATCTGCC CACTCCGCCT 120
CCCAAAGCCC CTGCGGCTCT TATCCATAGA TCCTGCACAG GAACACCCCC ACGCAGGCCC 180
TGGCCCTCTC CTTGTTATGT GTCCCTGAGG CTGTCCTCCC AGGACTTGGT TCACTTTCAG 240
GTCTGCCACC CATTGGTGCA TTCATTTCTG TATTTAATGT TACTGAGCAC CAACTATGTC 300
CCACACACTC TTCCAGGTAC TGGGGATACA GCAGAGCCAA ACAAAACCGA GAAAGTCTCT 360
GCCCTCAAGC TTTTATTGAA GGAGGGAAAT AGACAAAAGA GAAGCAAACA AACAAAAAAG 420
GTAAAATCAG AGGGTGGTAA AAGCTATGAA GGAAATAAAG CAGTATAACT GCTTAAGGAG 480
CAGGGACCTC TGCAGGTGGA TGGCAAGGGA AGGTCTCTCT GCAGAGACGA CATTGACATT 540
CATGCTGAGA CCTGGGCCAG CCATGCAAAG AAGGGGGGTG TAGGCAGAAG TGCCGCAGTG 600
GGAACAGGCT AGAAGTTGGG CCTGGTGCTG GGACAGTCCC AGTTCAGGCA TGTCCTCCTG 660
GTGTCGTTTT TAATAGCTCA TCCTTTCACA ATCAAGAGTG GCTCATGCCG GAGATGAGTT 720
ACCCGCAATG AGGGGCTGGA TTTATTCTAA GGGCAGAGGG AAGCCATCAC AGGAAATGAT 780
GTGATTGATG TTTTGAAAAG AACTCGCTGG CTGTTCCGTG AAGAATAAAT TAGAGGGGCA 840
GGAGGGAAGA AGTCTGCCTG GGGCGGCTGC AGCAACCCAG GCGTGCTGCG AGGTGCCCTT 900
TGACTAGATT CCAGTGGGGG CTTTCGGGCG AGCAGAAGAA CCCCAGGGAT CAGCTCTAGC 960
CACGCTCAGC TCCCTGGGCC GGCCCTGGGC ATTTCTGAGA CGGCCCTCGC GCTCAGGGAC 1020
CTCTCCTCGC AGTTCCATTG TCTGTTCTTG CGGAGTCCTG CCACACTGGG AGGGCCACCC 1080
CCTCCTCTTG CTCCCCTCCC CTCCCCGGGT CCAGCCCCTC CCCTGCCTGG CCCGGCTGCC 1140
GCCCAGCGCC AGCCAGAGCC CACCCCGCCT CCCTGCAGGA AGCCGGCTGG CGGCGCCTGC 1200
TGCGTGACCT TGGGCTGCAA AGTCGGGCGT TTGCAAAGTC AAAGCGAGTC ACTTCCTCCC 1260
CCAGGCCTCC CCCGAGCGGG CAGCCGGCCG CCGCTCCCTG CCCCCTCGCC CGCCGCGGGC 1320
CGGGGCTGGC GCTGGCACGA ACGCGCTCTG CATGCTAAGT GCTCGCGCCC GTTCCCGCCG 1380
CCCGGAGGCT CATTTGTCAC CCGCTGCTGA CTCAGCACTT CTGCAGAAGG CTTTTCCCTC 1440
CGCTTTGGAG GAGGAGGCCC GGAAATGAGG CAGAGGCTCT TCCTTCCCTT CCCTCCAGCA 1500
GGGGTGTGTG GCGTGGGTGT GTGCGGGTGT GGCAGGGTCT GTCTGTATGT CTGATGCCTG 1560
TCCATCACCG GTGTATATTT TCGCGGCTGT GTCTGTCTTT TGTGTATGGC TGAGTCTGTG 1620
TATGTGTCTT AGTGCATGTT GATCCCTGCG CCTGTCTGGT GGGTCTTTGT CCCTGTCTGT 1680
GGGCATCTGT GTTGGCCTGT GGGCCTGTCA TGTGTGTGTC ATACGTGTGT CTGGGTGAGT 1740
GTGTGTGTGT CCCCCCCACC CCCCTCCCTC AGCCCCAGCC TCCTCCCCTC AGACTTCACC 1800
TTGTCTCCTG GAGTGACCCT GGGGTTTCTG AGGCCAAAGT GGCACACCTT CCCTCCCCTG 1860
GCACCCCCAG CTCCCATCCC ACCCTCTGCC ACCAGTCCCC TAACATGGGA CCTCAGGGGC 1920
TGAAAACACA GGCTCTGGAA TCAGCCACAT CTCCACATCT AGGTCTCAGC CTAGGCTCTG 1980
CACTTGCCAC AGGGACCTTA AATGAGATAC CTTTCCTGAG CCTGTTTCCA CACTTATAAA 2040
ATAGAGGTGA TCATATCTCC CTAAAAGAGG ATAATTTCAT GATGGGGTCT GGTATATCAC 2100
ATGCAGCAAA TGGTGCCTGT TATTTCTACT TAAAGCAATA GGCCCAGTGT CAGGCACATA 2160
GCCAGGGTCT AATAAACGGC CACTTAAGAA TAAAAGCACC AAGAAGCCCT TTCCTTGGCT 2220
GCCAGAAAAG GGAGTGGGTG GGGAGATGGT GACCTGGATT GGGAGCTGGG CAGGAGCTGT 2280
TTGCATGACA CCTACTGTGA GGAGAGAGAT GTGGTGACCT GATTTAGTGC TGCCTTGGGC 2340
AGCCAAGGAA GTCAGGAAGG AAATCACAGA CGAGGGGCTC GGGAGCTGCT GTGCCCTGCC 2400
CTGCCCTTCC CCAGACCACA CACTGCCTGA CACCCGCAGG CAGAGTGAGG GCCCAGGGGG 2460
GAGGAGCACA ACTCCATGCC AGCCCCTACC TCCAGAGCAG CCCTCATGCT GTGTCCCTGG 2520
GTGAACAACT TTTTTTTTTT TTTTTTAAGA CAGGGTCTCT CTCAGCCACA TAGGCTCGAC 2580
TACAGTGGCG CGATCATAGC TCACTGCAGC TTCGACTTCG CGGGCTCAAA AGATTCTCCC 2640
CCTTCAGCCT CCTGAGTAAC TGGGACTACA GGTGCATGCC ACCATGCCCA GCTAATTTTT 2700
AATTTTTTTT TGAAGGGACA GGGTCTTGCT ATGTTGCCCA GGCTGGTCTT GAACTCCTGG 2760
GCTCAAGTGA TCCTCCTGCG TCTGCCTACT GAAGTCCTGG AATTATAGGC ATAAGCCACT 2820
TTGTCCAGCC GCTGGGAGAA TATGCACATC CATTCGTTTT ACCTCTTTAG CAATCTTGTG 2880
AAGGAGATTC TTAGCATCCC CATTTTGCAG CTGAGAAAAA CTGAGACTGG GAGGTTAAGT 2940
CCCAAGGTCA CAGGACCGAC AGGTGGCTGA GAGAACCCTG GCATTCCAGC TGCCAGTCAG 3000