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

TagContent
EnhancerAtlas ID
HS177-07096 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH_RA 
Coordinate
chr14:77421820-77424170 
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
CACTCCGCCT CCCAAAGCCC CTGCGGCTCT TATCCATAGA TCCTGCACAG GAACACCCCC 60
ACGCAGGCCC TGGCCCTCTC CTTGTTATGT GTCCCTGAGG CTGTCCTCCC AGGACTTGGT 120
TCACTTTCAG GTCTGCCACC CATTGGTGCA TTCATTTCTG TATTTAATGT TACTGAGCAC 180
CAACTATGTC CCACACACTC TTCCAGGTAC TGGGGATACA GCAGAGCCAA ACAAAACCGA 240
GAAAGTCTCT GCCCTCAAGC TTTTATTGAA GGAGGGAAAT AGACAAAAGA GAAGCAAACA 300
AACAAAAAAG GTAAAATCAG AGGGTGGTAA AAGCTATGAA GGAAATAAAG CAGTATAACT 360
GCTTAAGGAG CAGGGACCTC TGCAGGTGGA TGGCAAGGGA AGGTCTCTCT GCAGAGACGA 420
CATTGACATT CATGCTGAGA CCTGGGCCAG CCATGCAAAG AAGGGGGGTG TAGGCAGAAG 480
TGCCGCAGTG GGAACAGGCT AGAAGTTGGG CCTGGTGCTG GGACAGTCCC AGTTCAGGCA 540
TGTCCTCCTG GTGTCGTTTT TAATAGCTCA TCCTTTCACA ATCAAGAGTG GCTCATGCCG 600
GAGATGAGTT ACCCGCAATG AGGGGCTGGA TTTATTCTAA GGGCAGAGGG AAGCCATCAC 660
AGGAAATGAT GTGATTGATG TTTTGAAAAG AACTCGCTGG CTGTTCCGTG AAGAATAAAT 720
TAGAGGGGCA GGAGGGAAGA AGTCTGCCTG GGGCGGCTGC AGCAACCCAG GCGTGCTGCG 780
AGGTGCCCTT TGACTAGATT CCAGTGGGGG CTTTCGGGCG AGCAGAAGAA CCCCAGGGAT 840
CAGCTCTAGC CACGCTCAGC TCCCTGGGCC GGCCCTGGGC ATTTCTGAGA CGGCCCTCGC 900
GCTCAGGGAC CTCTCCTCGC AGTTCCATTG TCTGTTCTTG CGGAGTCCTG CCACACTGGG 960
AGGGCCACCC CCTCCTCTTG CTCCCCTCCC CTCCCCGGGT CCAGCCCCTC CCCTGCCTGG 1020
CCCGGCTGCC GCCCAGCGCC AGCCAGAGCC CACCCCGCCT CCCTGCAGGA AGCCGGCTGG 1080
CGGCGCCTGC TGCGTGACCT TGGGCTGCAA AGTCGGGCGT TTGCAAAGTC AAAGCGAGTC 1140
ACTTCCTCCC CCAGGCCTCC CCCGAGCGGG CAGCCGGCCG CCGCTCCCTG CCCCCTCGCC 1200
CGCCGCGGGC CGGGGCTGGC GCTGGCACGA ACGCGCTCTG CATGCTAAGT GCTCGCGCCC 1260
GTTCCCGCCG CCCGGAGGCT CATTTGTCAC CCGCTGCTGA CTCAGCACTT CTGCAGAAGG 1320
CTTTTCCCTC CGCTTTGGAG GAGGAGGCCC GGAAATGAGG CAGAGGCTCT TCCTTCCCTT 1380
CCCTCCAGCA GGGGTGTGTG GCGTGGGTGT GTGCGGGTGT GGCAGGGTCT GTCTGTATGT 1440
CTGATGCCTG TCCATCACCG GTGTATATTT TCGCGGCTGT GTCTGTCTTT TGTGTATGGC 1500
TGAGTCTGTG TATGTGTCTT AGTGCATGTT GATCCCTGCG CCTGTCTGGT GGGTCTTTGT 1560
CCCTGTCTGT GGGCATCTGT GTTGGCCTGT GGGCCTGTCA TGTGTGTGTC ATACGTGTGT 1620
CTGGGTGAGT GTGTGTGTGT CCCCCCCACC CCCCTCCCTC AGCCCCAGCC TCCTCCCCTC 1680
AGACTTCACC TTGTCTCCTG GAGTGACCCT GGGGTTTCTG AGGCCAAAGT GGCACACCTT 1740
CCCTCCCCTG GCACCCCCAG CTCCCATCCC ACCCTCTGCC ACCAGTCCCC TAACATGGGA 1800
CCTCAGGGGC TGAAAACACA GGCTCTGGAA TCAGCCACAT CTCCACATCT AGGTCTCAGC 1860
CTAGGCTCTG CACTTGCCAC AGGGACCTTA AATGAGATAC CTTTCCTGAG CCTGTTTCCA 1920
CACTTATAAA ATAGAGGTGA TCATATCTCC CTAAAAGAGG ATAATTTCAT GATGGGGTCT 1980
GGTATATCAC ATGCAGCAAA TGGTGCCTGT TATTTCTACT TAAAGCAATA GGCCCAGTGT 2040
CAGGCACATA GCCAGGGTCT AATAAACGGC CACTTAAGAA TAAAAGCACC AAGAAGCCCT 2100
TTCCTTGGCT GCCAGAAAAG GGAGTGGGTG GGGAGATGGT GACCTGGATT GGGAGCTGGG 2160
CAGGAGCTGT TTGCATGACA CCTACTGTGA GGAGAGAGAT GTGGTGACCT GATTTAGTGC 2220
TGCCTTGGGC AGCCAAGGAA GTCAGGAAGG AAATCACAGA CGAGGGGCTC GGGAGCTGCT 2280
GTGCCCTGCC CTGCCCTTCC CCAGACCACA CACTGCCTGA CACCCGCAGG CAGAGTGAGG 2340
GCCCAGGGGG 2350