EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-09586 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr14:105142390-105144030 
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
GAAGCTCCAT GTGCTGCAAC ACAAGTTATA TGTCCTGACA TGGATGCCTT GCTGGGGGTG 60
GTGGGGGGTG ATTCGCCTGC AGACGTCAAA GCCCTGCCTG CCAAGATCCT TGACTTCCCA 120
GCCCCAACCA GGCATCACTC AAAGGTGACC TCTCCACTCC CAGCACCAAG GAGTTGCCTT 180
TGGACCCTGA CCACCCTGAT GGCCAAGGCT AGGCTGGCCA GCACCTCCCC AGCAGCCCTT 240
CAGAGGCCTC CACAGCCCTG TGTCCAGTCT GACACAAGTG TGTCAGGTGG TCATGAGCAC 300
CGTTCCCTTC CAGCAAGGCC ACCTCTTCCT GTGGGGAAGG GCCTCAGGTA GGCAGGCCGG 360
AAGCACCTGC AGACCCCGCA CTCAGAAACT GCCACCCCGC TTGTTGAACC TTGTGTTTTA 420
GAAAGGGTCT TCCTTTCACA GCATCTCCCT CTCCCCAGTC CTCCTCCCAG AGGCTGTTTA 480
AGGGTGGGCG TGGGACCCCC AGTGTTTCCA GGGTTATTCC TAGGGATGGA CTTCTTATAA 540
ACAATATTGC CCCTCTTCCC AGGGCCCCAG GGCAAGGAGC AGCGAGCCTG GACCTGCAGC 600
CACTGTAGCC CCAGCCTGGG GGAGGGGACA GCACAATCAG GGTGAAGTGG AGTCAGAGGT 660
GGGTGTTGTG GAGGGGGGAG CGGCGCGGGG ACAGCTGTCC TGGCCCGGCT ACCTTCCCTG 720
CCCCCTGTGA CATCAGCCCA TCAATTCCCT CCCTCTTTTG CCCTCACTAG GTCGGGTCTC 780
TGGCCCTCGC AGCCACAAGG TTCCTGACTC CTGTGTCCTT GTGAAAGAGC CACACACAGC 840
AGCAGGGGGA CTGCCCCCGC CAGGACCAGC CCAGGATTCC TGCTGGATTC CGTGTGTCAG 900
GACCACCCAT TCTAGCAGAG GAGCAGGAAG CCCAGAGAGG CAAATCACGC GTCTAGGAAG 960
CAGAGAGGGA TCCCCGCCCC AGGGCCGCCT GAGGAGTGAG AGAGCTGAGG CTGAGGTCTG 1020
CTGTTACTAG AGCTGAAACC TACGGACCTA CCCAGCTCCC GTTTTCGCCG CTGGGGAGAC 1080
CCACGGGGAG ATCAAGGGGC CTGGGGGGGG GGGGGCCCTC CCACCTTGGA CGTTGGTTGC 1140
CACATCTGCA CGTGACGGGG AGAAACGTGT CATTCCAGGA GGACAGGAGG GCGGGGCAGC 1200
TGAGGGGGGA TCCCCAGATA TAGGGGCATC CCCAGGACCC ACCCCCGTCC TGTGGAGGCA 1260
GGAGGAGGGG CCGCACCCCT GGGTTTGAAA GGCAGCAGCC GCCTTCCAGA GGGAGCGCTG 1320
GCGGGACCTT ACCGCACCCC CTTCAGAGTA GCCCCCTCCC CCCATTGCTG CCCTGGACTC 1380
TGCGGCCAGC AAGCTGGAGG TTCCTAGGGC TATGGGGGAC AGGAGGCTGT GGCTGGCTGA 1440
GGACTTTGTG TCAATGTTCC CACTGCCTCT GGGGACTGGG GACAGCCAGG CCACACGCGG 1500
GGGCAGTGGG ACTTAGCACC TGAGCCTGCT GAGCTCCTGA AAGCCCTGGA GGTTCTCGGT 1560
TCCCCGAGGT GGGGCAGGGA GGAGGGAGCC CCTGGTGTGG CCTGGTTCTG CTGGGCGGAA 1620
CACTCAACAC TCCCTTCCCT 1640