EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-18122 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr14:77421680-77424220 
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: 1             
ChromosomeStartEnd
chr147742224077422571
Enhancer Sequence
TCTCTTGCCT CAGCCTCCTG AGTAGCTGGG ATTACAGGCG CCCGCCACCA CGCCTGGCTA 60
AATTTTGTAT TTTTAGTAGA GACGAGGTTT CACCATGTTG GCCAGGCTGG TCTCGAACTC 120
CTGACCTAAG GTGATCTGCC CACTCCGCCT CCCAAAGCCC CTGCGGCTCT TATCCATAGA 180
TCCTGCACAG GAACACCCCC ACGCAGGCCC TGGCCCTCTC CTTGTTATGT GTCCCTGAGG 240
CTGTCCTCCC AGGACTTGGT TCACTTTCAG GTCTGCCACC CATTGGTGCA TTCATTTCTG 300
TATTTAATGT TACTGAGCAC CAACTATGTC CCACACACTC TTCCAGGTAC TGGGGATACA 360
GCAGAGCCAA ACAAAACCGA GAAAGTCTCT GCCCTCAAGC TTTTATTGAA GGAGGGAAAT 420
AGACAAAAGA GAAGCAAACA AACAAAAAAG GTAAAATCAG AGGGTGGTAA AAGCTATGAA 480
GGAAATAAAG CAGTATAACT GCTTAAGGAG CAGGGACCTC TGCAGGTGGA TGGCAAGGGA 540
AGGTCTCTCT GCAGAGACGA CATTGACATT CATGCTGAGA CCTGGGCCAG CCATGCAAAG 600
AAGGGGGGTG TAGGCAGAAG TGCCGCAGTG GGAACAGGCT AGAAGTTGGG CCTGGTGCTG 660
GGACAGTCCC AGTTCAGGCA TGTCCTCCTG GTGTCGTTTT TAATAGCTCA TCCTTTCACA 720
ATCAAGAGTG GCTCATGCCG GAGATGAGTT ACCCGCAATG AGGGGCTGGA TTTATTCTAA 780
GGGCAGAGGG AAGCCATCAC AGGAAATGAT GTGATTGATG TTTTGAAAAG AACTCGCTGG 840
CTGTTCCGTG AAGAATAAAT TAGAGGGGCA GGAGGGAAGA AGTCTGCCTG GGGCGGCTGC 900
AGCAACCCAG GCGTGCTGCG AGGTGCCCTT TGACTAGATT CCAGTGGGGG CTTTCGGGCG 960
AGCAGAAGAA CCCCAGGGAT CAGCTCTAGC CACGCTCAGC TCCCTGGGCC GGCCCTGGGC 1020
ATTTCTGAGA CGGCCCTCGC GCTCAGGGAC CTCTCCTCGC AGTTCCATTG TCTGTTCTTG 1080
CGGAGTCCTG CCACACTGGG AGGGCCACCC CCTCCTCTTG CTCCCCTCCC CTCCCCGGGT 1140
CCAGCCCCTC CCCTGCCTGG CCCGGCTGCC GCCCAGCGCC AGCCAGAGCC CACCCCGCCT 1200
CCCTGCAGGA AGCCGGCTGG CGGCGCCTGC TGCGTGACCT TGGGCTGCAA AGTCGGGCGT 1260
TTGCAAAGTC AAAGCGAGTC ACTTCCTCCC CCAGGCCTCC CCCGAGCGGG CAGCCGGCCG 1320
CCGCTCCCTG CCCCCTCGCC CGCCGCGGGC CGGGGCTGGC GCTGGCACGA ACGCGCTCTG 1380
CATGCTAAGT GCTCGCGCCC GTTCCCGCCG CCCGGAGGCT CATTTGTCAC CCGCTGCTGA 1440
CTCAGCACTT CTGCAGAAGG CTTTTCCCTC CGCTTTGGAG GAGGAGGCCC GGAAATGAGG 1500
CAGAGGCTCT TCCTTCCCTT CCCTCCAGCA GGGGTGTGTG GCGTGGGTGT GTGCGGGTGT 1560
GGCAGGGTCT GTCTGTATGT CTGATGCCTG TCCATCACCG GTGTATATTT TCGCGGCTGT 1620
GTCTGTCTTT TGTGTATGGC TGAGTCTGTG TATGTGTCTT AGTGCATGTT GATCCCTGCG 1680
CCTGTCTGGT GGGTCTTTGT CCCTGTCTGT GGGCATCTGT GTTGGCCTGT GGGCCTGTCA 1740
TGTGTGTGTC ATACGTGTGT CTGGGTGAGT GTGTGTGTGT CCCCCCCACC CCCCTCCCTC 1800
AGCCCCAGCC TCCTCCCCTC AGACTTCACC TTGTCTCCTG GAGTGACCCT GGGGTTTCTG 1860
AGGCCAAAGT GGCACACCTT CCCTCCCCTG GCACCCCCAG CTCCCATCCC ACCCTCTGCC 1920
ACCAGTCCCC TAACATGGGA CCTCAGGGGC TGAAAACACA GGCTCTGGAA TCAGCCACAT 1980
CTCCACATCT AGGTCTCAGC CTAGGCTCTG CACTTGCCAC AGGGACCTTA AATGAGATAC 2040
CTTTCCTGAG CCTGTTTCCA CACTTATAAA ATAGAGGTGA TCATATCTCC CTAAAAGAGG 2100
ATAATTTCAT GATGGGGTCT GGTATATCAC ATGCAGCAAA TGGTGCCTGT TATTTCTACT 2160
TAAAGCAATA GGCCCAGTGT CAGGCACATA GCCAGGGTCT AATAAACGGC CACTTAAGAA 2220
TAAAAGCACC AAGAAGCCCT TTCCTTGGCT GCCAGAAAAG GGAGTGGGTG GGGAGATGGT 2280
GACCTGGATT GGGAGCTGGG CAGGAGCTGT TTGCATGACA CCTACTGTGA GGAGAGAGAT 2340
GTGGTGACCT GATTTAGTGC TGCCTTGGGC AGCCAAGGAA GTCAGGAAGG AAATCACAGA 2400
CGAGGGGCTC GGGAGCTGCT GTGCCCTGCC CTGCCCTTCC CCAGACCACA CACTGCCTGA 2460
CACCCGCAGG CAGAGTGAGG GCCCAGGGGG GAGGAGCACA ACTCCATGCC AGCCCCTACC 2520
TCCAGAGCAG CCCTCATGCT 2540