EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS001-02799 
Organism
Homo sapiens 
Tissue/cell
786-O 
Coordinate
chr14:105142380-105144030 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxq1MA0040.1chr14:105142925-105142936TATAAACAATA-6.32
RREB1MA0073.1chr14:105142438-105142458TTGCTGGGGGTGGTGGGGGG-6.83
ZNF263MA0528.1chr14:105142833-105142854TCTCCCTCTCCCCAGTCCTCC-6.37
ZNF263MA0528.1chr14:105142836-105142857CCCTCTCCCCAGTCCTCCTCC-7.67
ZNF740MA0753.2chr14:105143492-105143505GGGGGGGGGGGGG-6.03
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_01268chr14:105142926-105145260Adrenal_Gland
SE_03314chr14:105143585-105145203Brain_Angular_Gyrus
SE_04002chr14:105142206-105149771Brain_Anterior_Caudate
SE_04914chr14:105141940-105150616Brain_Cingulate_Gyrus
SE_06613chr14:105141624-105150853Brain_Hippocampus_Middle
SE_06789chr14:105142882-105149935Brain_Hippocampus_Middle_150
SE_07942chr14:105142379-105150029Brain_Inferior_Temporal_Lobe
SE_10261chr14:105143785-105145145CD19_Primary
SE_11342chr14:105143533-105145581CD20
SE_23154chr14:105143164-105149340Colon_Crypt_1
SE_23853chr14:105143505-105145548Colon_Crypt_2
SE_24738chr14:105142887-105149138Colon_Crypt_3
SE_27594chr14:105143038-105145374Esophagus
SE_28477chr14:105143343-105145550Fetal_Intestine
SE_31571chr14:105142931-105149890Gastric
SE_33152chr14:105142911-105143484H1
SE_33152chr14:105143602-105145292H1
SE_34297chr14:105142849-105150104HCT-116
SE_34783chr14:105143347-105150285HeLa
SE_42985chr14:105142854-105149438Lung
SE_47300chr14:105142661-105150462Panc1
SE_50435chr14:105142860-105149428Sigmoid_Colon
SE_52674chr14:105143028-105149527Small_Intestine
SE_56774chr14:105143497-105145611VACO_400
SE_65469chr14:105142505-105149535Pancreatic_islets
SE_68794chr14:105142813-105150105H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14105142577105142814
Enhancer Sequence
CCAGCAAGAG GAAGCTCCAT GTGCTGCAAC ACAAGTTATA TGTCCTGACA TGGATGCCTT 60
GCTGGGGGTG GTGGGGGGTG ATTCGCCTGC AGACGTCAAA GCCCTGCCTG CCAAGATCCT 120
TGACTTCCCA GCCCCAACCA GGCATCACTC AAAGGTGACC TCTCCACTCC CAGCACCAAG 180
GAGTTGCCTT TGGACCCTGA CCACCCTGAT GGCCAAGGCT AGGCTGGCCA GCACCTCCCC 240
AGCAGCCCTT CAGAGGCCTC CACAGCCCTG TGTCCAGTCT GACACAAGTG TGTCAGGTGG 300
TCATGAGCAC CGTTCCCTTC CAGCAAGGCC ACCTCTTCCT GTGGGGAAGG GCCTCAGGTA 360
GGCAGGCCGG AAGCACCTGC AGACCCCGCA CTCAGAAACT GCCACCCCGC TTGTTGAACC 420
TTGTGTTTTA GAAAGGGTCT TCCTTTCACA GCATCTCCCT CTCCCCAGTC CTCCTCCCAG 480
AGGCTGTTTA AGGGTGGGCG TGGGACCCCC AGTGTTTCCA GGGTTATTCC TAGGGATGGA 540
CTTCTTATAA ACAATATTGC CCCTCTTCCC AGGGCCCCAG GGCAAGGAGC AGCGAGCCTG 600
GACCTGCAGC CACTGTAGCC CCAGCCTGGG GGAGGGGACA GCACAATCAG GGTGAAGTGG 660
AGTCAGAGGT GGGTGTTGTG GAGGGGGGAG CGGCGCGGGG ACAGCTGTCC TGGCCCGGCT 720
ACCTTCCCTG CCCCCTGTGA CATCAGCCCA TCAATTCCCT CCCTCTTTTG CCCTCACTAG 780
GTCGGGTCTC TGGCCCTCGC AGCCACAAGG TTCCTGACTC CTGTGTCCTT GTGAAAGAGC 840
CACACACAGC AGCAGGGGGA CTGCCCCCGC CAGGACCAGC CCAGGATTCC TGCTGGATTC 900
CGTGTGTCAG GACCACCCAT TCTAGCAGAG GAGCAGGAAG CCCAGAGAGG CAAATCACGC 960
GTCTAGGAAG CAGAGAGGGA TCCCCGCCCC AGGGCCGCCT GAGGAGTGAG AGAGCTGAGG 1020
CTGAGGTCTG CTGTTACTAG AGCTGAAACC TACGGACCTA CCCAGCTCCC GTTTTCGCCG 1080
CTGGGGAGAC CCACGGGGAG ATCAAGGGGC CTGGGGGGGG GGGGGCCCTC CCACCTTGGA 1140
CGTTGGTTGC CACATCTGCA CGTGACGGGG AGAAACGTGT CATTCCAGGA GGACAGGAGG 1200
GCGGGGCAGC TGAGGGGGGA TCCCCAGATA TAGGGGCATC CCCAGGACCC ACCCCCGTCC 1260
TGTGGAGGCA GGAGGAGGGG CCGCACCCCT GGGTTTGAAA GGCAGCAGCC GCCTTCCAGA 1320
GGGAGCGCTG GCGGGACCTT ACCGCACCCC CTTCAGAGTA GCCCCCTCCC CCCATTGCTG 1380
CCCTGGACTC TGCGGCCAGC AAGCTGGAGG TTCCTAGGGC TATGGGGGAC AGGAGGCTGT 1440
GGCTGGCTGA GGACTTTGTG TCAATGTTCC CACTGCCTCT GGGGACTGGG GACAGCCAGG 1500
CCACACGCGG GGGCAGTGGG ACTTAGCACC TGAGCCTGCT GAGCTCCTGA AAGCCCTGGA 1560
GGTTCTCGGT TCCCCGAGGT GGGGCAGGGA GGAGGGAGCC CCTGGTGTGG CCTGGTTCTG 1620
CTGGGCGGAA CACTCAACAC TCCCTTCCCT 1650