EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-12395 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr14:77421690-77424360 
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
CAGCCTCCTG AGTAGCTGGG ATTACAGGCG CCCGCCACCA CGCCTGGCTA AATTTTGTAT 60
TTTTAGTAGA GACGAGGTTT CACCATGTTG GCCAGGCTGG TCTCGAACTC CTGACCTAAG 120
GTGATCTGCC CACTCCGCCT CCCAAAGCCC CTGCGGCTCT TATCCATAGA TCCTGCACAG 180
GAACACCCCC ACGCAGGCCC TGGCCCTCTC CTTGTTATGT GTCCCTGAGG CTGTCCTCCC 240
AGGACTTGGT TCACTTTCAG GTCTGCCACC CATTGGTGCA TTCATTTCTG TATTTAATGT 300
TACTGAGCAC CAACTATGTC CCACACACTC TTCCAGGTAC TGGGGATACA GCAGAGCCAA 360
ACAAAACCGA GAAAGTCTCT GCCCTCAAGC TTTTATTGAA GGAGGGAAAT AGACAAAAGA 420
GAAGCAAACA AACAAAAAAG GTAAAATCAG AGGGTGGTAA AAGCTATGAA GGAAATAAAG 480
CAGTATAACT GCTTAAGGAG CAGGGACCTC TGCAGGTGGA TGGCAAGGGA AGGTCTCTCT 540
GCAGAGACGA CATTGACATT CATGCTGAGA CCTGGGCCAG CCATGCAAAG AAGGGGGGTG 600
TAGGCAGAAG TGCCGCAGTG GGAACAGGCT AGAAGTTGGG CCTGGTGCTG GGACAGTCCC 660
AGTTCAGGCA TGTCCTCCTG GTGTCGTTTT TAATAGCTCA TCCTTTCACA ATCAAGAGTG 720
GCTCATGCCG GAGATGAGTT ACCCGCAATG AGGGGCTGGA TTTATTCTAA GGGCAGAGGG 780
AAGCCATCAC AGGAAATGAT GTGATTGATG TTTTGAAAAG AACTCGCTGG CTGTTCCGTG 840
AAGAATAAAT TAGAGGGGCA GGAGGGAAGA AGTCTGCCTG GGGCGGCTGC AGCAACCCAG 900
GCGTGCTGCG AGGTGCCCTT TGACTAGATT CCAGTGGGGG CTTTCGGGCG AGCAGAAGAA 960
CCCCAGGGAT CAGCTCTAGC CACGCTCAGC TCCCTGGGCC GGCCCTGGGC ATTTCTGAGA 1020
CGGCCCTCGC GCTCAGGGAC CTCTCCTCGC AGTTCCATTG TCTGTTCTTG CGGAGTCCTG 1080
CCACACTGGG AGGGCCACCC CCTCCTCTTG CTCCCCTCCC CTCCCCGGGT CCAGCCCCTC 1140
CCCTGCCTGG CCCGGCTGCC GCCCAGCGCC AGCCAGAGCC CACCCCGCCT CCCTGCAGGA 1200
AGCCGGCTGG CGGCGCCTGC TGCGTGACCT TGGGCTGCAA AGTCGGGCGT TTGCAAAGTC 1260
AAAGCGAGTC ACTTCCTCCC CCAGGCCTCC CCCGAGCGGG CAGCCGGCCG CCGCTCCCTG 1320
CCCCCTCGCC CGCCGCGGGC CGGGGCTGGC GCTGGCACGA ACGCGCTCTG CATGCTAAGT 1380
GCTCGCGCCC GTTCCCGCCG CCCGGAGGCT CATTTGTCAC CCGCTGCTGA CTCAGCACTT 1440
CTGCAGAAGG CTTTTCCCTC CGCTTTGGAG GAGGAGGCCC GGAAATGAGG CAGAGGCTCT 1500
TCCTTCCCTT CCCTCCAGCA GGGGTGTGTG GCGTGGGTGT GTGCGGGTGT GGCAGGGTCT 1560
GTCTGTATGT CTGATGCCTG TCCATCACCG GTGTATATTT TCGCGGCTGT GTCTGTCTTT 1620
TGTGTATGGC TGAGTCTGTG TATGTGTCTT AGTGCATGTT GATCCCTGCG CCTGTCTGGT 1680
GGGTCTTTGT CCCTGTCTGT GGGCATCTGT GTTGGCCTGT GGGCCTGTCA TGTGTGTGTC 1740
ATACGTGTGT CTGGGTGAGT GTGTGTGTGT CCCCCCCACC CCCCTCCCTC AGCCCCAGCC 1800
TCCTCCCCTC AGACTTCACC TTGTCTCCTG GAGTGACCCT GGGGTTTCTG AGGCCAAAGT 1860
GGCACACCTT CCCTCCCCTG GCACCCCCAG CTCCCATCCC ACCCTCTGCC ACCAGTCCCC 1920
TAACATGGGA CCTCAGGGGC TGAAAACACA GGCTCTGGAA TCAGCCACAT CTCCACATCT 1980
AGGTCTCAGC CTAGGCTCTG CACTTGCCAC AGGGACCTTA AATGAGATAC CTTTCCTGAG 2040
CCTGTTTCCA CACTTATAAA ATAGAGGTGA TCATATCTCC CTAAAAGAGG ATAATTTCAT 2100
GATGGGGTCT GGTATATCAC ATGCAGCAAA TGGTGCCTGT TATTTCTACT TAAAGCAATA 2160
GGCCCAGTGT CAGGCACATA GCCAGGGTCT AATAAACGGC CACTTAAGAA TAAAAGCACC 2220
AAGAAGCCCT TTCCTTGGCT GCCAGAAAAG GGAGTGGGTG GGGAGATGGT GACCTGGATT 2280
GGGAGCTGGG CAGGAGCTGT TTGCATGACA CCTACTGTGA GGAGAGAGAT GTGGTGACCT 2340
GATTTAGTGC TGCCTTGGGC AGCCAAGGAA GTCAGGAAGG AAATCACAGA CGAGGGGCTC 2400
GGGAGCTGCT GTGCCCTGCC CTGCCCTTCC CCAGACCACA CACTGCCTGA CACCCGCAGG 2460
CAGAGTGAGG GCCCAGGGGG GAGGAGCACA ACTCCATGCC AGCCCCTACC TCCAGAGCAG 2520
CCCTCATGCT GTGTCCCTGG GTGAACAACT TTTTTTTTTT TTTTTTAAGA CAGGGTCTCT 2580
CTCAGCCACA TAGGCTCGAC TACAGTGGCG CGATCATAGC TCACTGCAGC TTCGACTTCG 2640
CGGGCTCAAA AGATTCTCCC CCTTCAGCCT 2670