EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS036-00946 
Organism
Homo sapiens 
Tissue/cell
endometrioid_adenocarcinoma 
Coordinate
chr14:35804490-35807060 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr14:35807039-35807057CTTGCCTCCCTTCCTTTC-6.46
EWSR1-FLI1MA0149.1chr14:35804787-35804805CCTCCCTTCCTTGGTTCC-6.54
EWSR1-FLI1MA0149.1chr14:35804779-35804797CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr14:35804775-35804793CCTTCCTCCCTCCCTCCC-7.28
EWSR1-FLI1MA0149.1chr14:35804771-35804789TCTTCCTTCCTCCCTCCC-7.39
EWSR1-FLI1MA0149.1chr14:35804795-35804813CCTTGGTTCCTTCCTTCC-7.95
EWSR1-FLI1MA0149.1chr14:35804791-35804809CCTTCCTTGGTTCCTTCC-7.97
GATA2MA0036.3chr14:35804919-35804930TTCTTATCTTC+6.02
ZNF263MA0528.1chr14:35804774-35804795TCCTTCCTCCCTCCCTCCCTT-6.46
Number of super-enhancer constituents: 21             
IDCoordinateTissue/cell
SE_01165chr14:35804585-35807755Adrenal_Gland
SE_23298chr14:35804386-35805475Colon_Crypt_1
SE_23298chr14:35805483-35807654Colon_Crypt_1
SE_24327chr14:35804571-35805314Colon_Crypt_2
SE_24327chr14:35805505-35807540Colon_Crypt_2
SE_26613chr14:35804098-35807686Esophagus
SE_27693chr14:35800617-35807759Fetal_Intestine
SE_28626chr14:35800494-35807947Fetal_Intestine_Large
SE_32027chr14:35804417-35807628Gastric
SE_34130chr14:35804231-35807631HCC1954
SE_34831chr14:35800577-35808006HeLa
SE_41762chr14:35804426-35805281LNCaP
SE_41762chr14:35805560-35807508LNCaP
SE_42211chr14:35804395-35807731Lung
SE_47013chr14:35804472-35805292Ovary
SE_47013chr14:35805519-35807575Ovary
SE_49399chr14:35804402-35805395Right_Atrium
SE_49399chr14:35805440-35807651Right_Atrium
SE_50091chr14:35804226-35807720Sigmoid_Colon
SE_52425chr14:35800645-35807722Small_Intestine
SE_53368chr14:35804110-35812246Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr143580568335806194
chr143580555735806834
Number: 1             
IDChromosomeStartEnd
GH14I035330chr143579998035812312
Enhancer Sequence
CCCAAAGTGC TAGGATTACA AGCGTGAGCC ACCCGGCCCA CTATTCCAGT TATTTTAAGA 60
TGTACATAAA TTATTATGTT ATCATACACT AGATTTTATT GAATCTACCA TTTCACATTC 120
TTATTGAGAG TGTAACCTCT TGAAGCCTAC TGGTGCAGGA GGGATTTTGC AACCTTCCTT 180
TGGCTTTTGT CACCTATGGA AAACTACAAA CCAGCTTGCC TATCCGGTGA TTGGAACCAG 240
GAGGATTGCC GGCCTTGGGT CTGGAAATCC TATCCCATGT GTCTTCCTTC CTCCCTCCCT 300
CCCTTCCTTG GTTCCTTCCT TCCCCTGACT AGGCCCCAGA GGGGTGGGGA GGCCTTCCTG 360
GGCCTGGCAT CAGGGCTCCT GGGCTCCCAG CCAAGTGTCC AGAGGTCACT CCTCCTGGCA 420
TCTGGATCCT TCTTATCTTC CTGAGACATA GGAGGCTCCT GCTCTGGAGA TGACTGAAGG 480
GAAAACACCT GTATTTCCAG GGCCTTGGAA ATAGCCTGCT CCAGCCGGCC TTCCCGGGAG 540
AAACTGAGAA AGGACATTGG TCCGAAGCAT TTCTCTTTCG GTTTGTGCTG CGCTGAGCCT 600
GTCCTGTGAT GCGGCCCTCA CCAACCAAGG ACTGAACGAG AGGGACTCCA TGCGAACCTG 660
CTCAGCATAC AGCAGGTGCC TCGTGGATAT TCTTCCCTAA GGCTCCAGGC CAGCCAAGCA 720
CTGCATTAAC CAGGTTCGGA TGAACTTTAG AATGTACGCA TCTGAGCTGT CATAGTTTTT 780
TGTTTTCTTG TTTTTTTGAG ATGGAGTTTC GCTCTTTCAC CCAGGCTGGA GTGAAATGCC 840
GCGATCTCAG CTCACTGCAA CCTCTGCCTC CTGGGTTCAA GCCATTCTCC TGCCTCAGCC 900
TCCCAAGTAT CTGCGATTAC AGGCTCCTGC CACCATGTCC AGCTAATTTT TTGTATTTTT 960
AGTAGAGACA GGGTTTCACC ATGTTGGCCA GGCTGGTCTT GAATTCCTGA CCTCAGGTGA 1020
TCCACCCACC TCGGCCTCCC AAAATGCTGG GATTACAGGC ATGAACCACT CTACCTGACC 1080
CATAGTTCTT AAATTTAAAA TCTTGATATG CTGGTGGATA TGCAGCTTGA TTTCTTTAAG 1140
CCGACATGGC CTGACTTTTT CAGATTCTCA GCCTGTGTTG GAGGGCTGTT GAGTGTTCTT 1200
TCTATGCAGA AAGTACGCCT GCCGTCCTCT GTTTTGTAAT CGCCACCCCA TCCCTGCCCA 1260
ACACACACAC CCACACAGCC GCAGTTACGC CGGGTCCAGC AACGCACGAA CCAAGTGGAA 1320
GGTCAAGGGC TGGGGCTCCG TTTCCCTCCC CTTGAAGCTG TTTGGTTTGC TCTTGTCCCA 1380
GCCCCTGACT GAGCCGCCAG CCCAGAACGG GGGCAGCCCT CCCCCATGCA GTCAGGGCCA 1440
GAGGAGCATA ATATTGCCCC CCCGGGTGCA GCCTTAGGTG CAGGAGCGTT GGGAATTTTC 1500
CATCTTGCTC TGCAGCCTGG CTTCTTAGGT CATCGTCCTG CTGCTGACAT AGGCCTGGGT 1560
TGGGCGAGTT TCCTGCAGGT CAGCGAGGGC GCGGAGGCAG CGCCTGAGCC TGCTCAGGGC 1620
CTGGCTTCCT GCCTGCTGTG AGGAAGGGTG GAGGAGGGGT TCGAGGCCTC AACCATCCCT 1680
TGGCCCAGAG CCTCAGGCCA AGCAGCCTCC GCCTCTGCCC AGGCCTGTCT CCTCCCGGCC 1740
TCCTGCTCTC CTGTTTCCTA AAGCTTTCCC GCTGGGTGGC TCCCAGTTCT TCCAGAAATC 1800
CCCTCCAGGA AATTTGCTTG TTGCCACAAA ATAATGCAAA TCTGTTCCTG GGGCCGCCCA 1860
GGCAACCTGC AGTCTCTGTC TCCCCAAGAC CTGAGGAGGG AGGGCGAGGC AGGCCCTGTG 1920
CCCGTCAGGG TCCCTTTTCC AGCCATGAGG ACAAAGGATA AGCCGCACCC TCGTCACCCT 1980
CTCATAAGCT GCAAGAGAAA GTTCCTGGTT TTACCTCTAA GGGAACCAGC TCCACCTAGG 2040
GAAAGGCCAC ACAGGACCCT CAAAGGCACC AAGGTCTTTT TTCTATTTAA TATCTAAAAC 2100
AGTCTGAATA TATTAAAGTT TATGCTCATG TTTGGCATTT GTTTATCTGT TTCTCGAACT 2160
TCAACTCCCT GCCGTGTCTG GAGCAGAAAG TGAAGGCCCA TGGATAACAC TTCTGCGTGC 2220
CACAGTCCTA GGTGGTGACC AATGCAGGGA TGCACAGGTG CCGTGTGGCC TTCTGCAGGC 2280
CAGGCCCCAC AGAGACCCAC AGTCAAGGTG GCCTGAGACC CTTGAACAAG GAGCTTGTGG 2340
CCAGAGAAAG GCTAAATGCA GCACCCCCAC CCCTGTGGCT AGTGCCAGGG CCCCACCTGA 2400
ATGCTCTGCA GTTGGGTCCC CCCAGGCCAT CTCCAGAGGA GAACGCAAGT GGGCTAGGGA 2460
GGGAACAGAC CAGCCTGATG CAAAACCCTC TCAGCCCAGC ACAGCCCTCG TGTCCCTGGG 2520
CTGAGGGTCT GGGGAGAACA TCACTTGCTC TTGCCTCCCT TCCTTTCTTG 2570