EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS197-06925 
Organism
Homo sapiens 
Tissue/cell
ZR75-30 
Coordinate
chr14:105142200-105144030 
Target genes
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
TTTGGATTCA GTAAGAGGTT TTAACACTAA GCTGTCTTAA ATGCCCAAAT GACAGGGCCA 60
AGGTGGGAGT AAATGAAGTG CCAGCTGATG GGAAAACTCC CAGCTCTGAC ACCTCTCACC 120
ACCCCTGCGA CTCTCCTGCT CAGATTCTGA ATCTGTAAAA TGGGAATGCT TAGTGGTGCT 180
CCAGCAAGAG GAAGCTCCAT GTGCTGCAAC ACAAGTTATA TGTCCTGACA TGGATGCCTT 240
GCTGGGGGTG GTGGGGGGTG ATTCGCCTGC AGACGTCAAA GCCCTGCCTG CCAAGATCCT 300
TGACTTCCCA GCCCCAACCA GGCATCACTC AAAGGTGACC TCTCCACTCC CAGCACCAAG 360
GAGTTGCCTT TGGACCCTGA CCACCCTGAT GGCCAAGGCT AGGCTGGCCA GCACCTCCCC 420
AGCAGCCCTT CAGAGGCCTC CACAGCCCTG TGTCCAGTCT GACACAAGTG TGTCAGGTGG 480
TCATGAGCAC CGTTCCCTTC CAGCAAGGCC ACCTCTTCCT GTGGGGAAGG GCCTCAGGTA 540
GGCAGGCCGG AAGCACCTGC AGACCCCGCA CTCAGAAACT GCCACCCCGC TTGTTGAACC 600
TTGTGTTTTA GAAAGGGTCT TCCTTTCACA GCATCTCCCT CTCCCCAGTC CTCCTCCCAG 660
AGGCTGTTTA AGGGTGGGCG TGGGACCCCC AGTGTTTCCA GGGTTATTCC TAGGGATGGA 720
CTTCTTATAA ACAATATTGC CCCTCTTCCC AGGGCCCCAG GGCAAGGAGC AGCGAGCCTG 780
GACCTGCAGC CACTGTAGCC CCAGCCTGGG GGAGGGGACA GCACAATCAG GGTGAAGTGG 840
AGTCAGAGGT GGGTGTTGTG GAGGGGGGAG CGGCGCGGGG ACAGCTGTCC TGGCCCGGCT 900
ACCTTCCCTG CCCCCTGTGA CATCAGCCCA TCAATTCCCT CCCTCTTTTG CCCTCACTAG 960
GTCGGGTCTC TGGCCCTCGC AGCCACAAGG TTCCTGACTC CTGTGTCCTT GTGAAAGAGC 1020
CACACACAGC AGCAGGGGGA CTGCCCCCGC CAGGACCAGC CCAGGATTCC TGCTGGATTC 1080
CGTGTGTCAG GACCACCCAT TCTAGCAGAG GAGCAGGAAG CCCAGAGAGG CAAATCACGC 1140
GTCTAGGAAG CAGAGAGGGA TCCCCGCCCC AGGGCCGCCT GAGGAGTGAG AGAGCTGAGG 1200
CTGAGGTCTG CTGTTACTAG AGCTGAAACC TACGGACCTA CCCAGCTCCC GTTTTCGCCG 1260
CTGGGGAGAC CCACGGGGAG ATCAAGGGGC CTGGGGGGGG GGGGGCCCTC CCACCTTGGA 1320
CGTTGGTTGC CACATCTGCA CGTGACGGGG AGAAACGTGT CATTCCAGGA GGACAGGAGG 1380
GCGGGGCAGC TGAGGGGGGA TCCCCAGATA TAGGGGCATC CCCAGGACCC ACCCCCGTCC 1440
TGTGGAGGCA GGAGGAGGGG CCGCACCCCT GGGTTTGAAA GGCAGCAGCC GCCTTCCAGA 1500
GGGAGCGCTG GCGGGACCTT ACCGCACCCC CTTCAGAGTA GCCCCCTCCC CCCATTGCTG 1560
CCCTGGACTC TGCGGCCAGC AAGCTGGAGG TTCCTAGGGC TATGGGGGAC AGGAGGCTGT 1620
GGCTGGCTGA GGACTTTGTG TCAATGTTCC CACTGCCTCT GGGGACTGGG GACAGCCAGG 1680
CCACACGCGG GGGCAGTGGG ACTTAGCACC TGAGCCTGCT GAGCTCCTGA AAGCCCTGGA 1740
GGTTCTCGGT TCCCCGAGGT GGGGCAGGGA GGAGGGAGCC CCTGGTGTGG CCTGGTTCTG 1800
CTGGGCGGAA CACTCAACAC TCCCTTCCCT 1830