EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS139-16282 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr14:35804600-35807650 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr14:35807039-35807057CTTGCCTCCCTTCCTTTC-6.46
EWSR1-FLI1MA0149.1chr14:35804787-35804805CCTCCCTTCCTTGGTTCC-6.54
EWSR1-FLI1MA0149.1chr14:35807043-35807061CCTCCCTTCCTTTCTTGC-6.7
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: 3             
ChromosomeStartEnd
chr143580684935807494
chr143580568335806194
chr143580555735806834
Number: 1             
IDChromosomeStartEnd
GH14I035330chr143579998035812312
Enhancer Sequence
TTTCACATTC TTATTGAGAG TGTAACCTCT TGAAGCCTAC TGGTGCAGGA GGGATTTTGC 60
AACCTTCCTT TGGCTTTTGT CACCTATGGA AAACTACAAA CCAGCTTGCC TATCCGGTGA 120
TTGGAACCAG GAGGATTGCC GGCCTTGGGT CTGGAAATCC TATCCCATGT GTCTTCCTTC 180
CTCCCTCCCT CCCTTCCTTG GTTCCTTCCT TCCCCTGACT AGGCCCCAGA GGGGTGGGGA 240
GGCCTTCCTG GGCCTGGCAT CAGGGCTCCT GGGCTCCCAG CCAAGTGTCC AGAGGTCACT 300
CCTCCTGGCA TCTGGATCCT TCTTATCTTC CTGAGACATA GGAGGCTCCT GCTCTGGAGA 360
TGACTGAAGG GAAAACACCT GTATTTCCAG GGCCTTGGAA ATAGCCTGCT CCAGCCGGCC 420
TTCCCGGGAG AAACTGAGAA AGGACATTGG TCCGAAGCAT TTCTCTTTCG GTTTGTGCTG 480
CGCTGAGCCT GTCCTGTGAT GCGGCCCTCA CCAACCAAGG ACTGAACGAG AGGGACTCCA 540
TGCGAACCTG CTCAGCATAC AGCAGGTGCC TCGTGGATAT TCTTCCCTAA GGCTCCAGGC 600
CAGCCAAGCA CTGCATTAAC CAGGTTCGGA TGAACTTTAG AATGTACGCA TCTGAGCTGT 660
CATAGTTTTT TGTTTTCTTG TTTTTTTGAG ATGGAGTTTC GCTCTTTCAC CCAGGCTGGA 720
GTGAAATGCC GCGATCTCAG CTCACTGCAA CCTCTGCCTC CTGGGTTCAA GCCATTCTCC 780
TGCCTCAGCC TCCCAAGTAT CTGCGATTAC AGGCTCCTGC CACCATGTCC AGCTAATTTT 840
TTGTATTTTT AGTAGAGACA GGGTTTCACC ATGTTGGCCA GGCTGGTCTT GAATTCCTGA 900
CCTCAGGTGA TCCACCCACC TCGGCCTCCC AAAATGCTGG GATTACAGGC ATGAACCACT 960
CTACCTGACC CATAGTTCTT AAATTTAAAA TCTTGATATG CTGGTGGATA TGCAGCTTGA 1020
TTTCTTTAAG CCGACATGGC CTGACTTTTT CAGATTCTCA GCCTGTGTTG GAGGGCTGTT 1080
GAGTGTTCTT TCTATGCAGA AAGTACGCCT GCCGTCCTCT GTTTTGTAAT CGCCACCCCA 1140
TCCCTGCCCA ACACACACAC CCACACAGCC GCAGTTACGC CGGGTCCAGC AACGCACGAA 1200
CCAAGTGGAA GGTCAAGGGC TGGGGCTCCG TTTCCCTCCC CTTGAAGCTG TTTGGTTTGC 1260
TCTTGTCCCA GCCCCTGACT GAGCCGCCAG CCCAGAACGG GGGCAGCCCT CCCCCATGCA 1320
GTCAGGGCCA GAGGAGCATA ATATTGCCCC CCCGGGTGCA GCCTTAGGTG CAGGAGCGTT 1380
GGGAATTTTC CATCTTGCTC TGCAGCCTGG CTTCTTAGGT CATCGTCCTG CTGCTGACAT 1440
AGGCCTGGGT TGGGCGAGTT TCCTGCAGGT CAGCGAGGGC GCGGAGGCAG CGCCTGAGCC 1500
TGCTCAGGGC CTGGCTTCCT GCCTGCTGTG AGGAAGGGTG GAGGAGGGGT TCGAGGCCTC 1560
AACCATCCCT TGGCCCAGAG CCTCAGGCCA AGCAGCCTCC GCCTCTGCCC AGGCCTGTCT 1620
CCTCCCGGCC TCCTGCTCTC CTGTTTCCTA AAGCTTTCCC GCTGGGTGGC TCCCAGTTCT 1680
TCCAGAAATC CCCTCCAGGA AATTTGCTTG TTGCCACAAA ATAATGCAAA TCTGTTCCTG 1740
GGGCCGCCCA GGCAACCTGC AGTCTCTGTC TCCCCAAGAC CTGAGGAGGG AGGGCGAGGC 1800
AGGCCCTGTG CCCGTCAGGG TCCCTTTTCC AGCCATGAGG ACAAAGGATA AGCCGCACCC 1860
TCGTCACCCT CTCATAAGCT GCAAGAGAAA GTTCCTGGTT TTACCTCTAA GGGAACCAGC 1920
TCCACCTAGG GAAAGGCCAC ACAGGACCCT CAAAGGCACC AAGGTCTTTT TTCTATTTAA 1980
TATCTAAAAC AGTCTGAATA TATTAAAGTT TATGCTCATG TTTGGCATTT GTTTATCTGT 2040
TTCTCGAACT TCAACTCCCT GCCGTGTCTG GAGCAGAAAG TGAAGGCCCA TGGATAACAC 2100
TTCTGCGTGC CACAGTCCTA GGTGGTGACC AATGCAGGGA TGCACAGGTG CCGTGTGGCC 2160
TTCTGCAGGC CAGGCCCCAC AGAGACCCAC AGTCAAGGTG GCCTGAGACC CTTGAACAAG 2220
GAGCTTGTGG CCAGAGAAAG GCTAAATGCA GCACCCCCAC CCCTGTGGCT AGTGCCAGGG 2280
CCCCACCTGA ATGCTCTGCA GTTGGGTCCC CCCAGGCCAT CTCCAGAGGA GAACGCAAGT 2340
GGGCTAGGGA GGGAACAGAC CAGCCTGATG CAAAACCCTC TCAGCCCAGC ACAGCCCTCG 2400
TGTCCCTGGG CTGAGGGTCT GGGGAGAACA TCACTTGCTC TTGCCTCCCT TCCTTTCTTG 2460
CTGCTGCTGC CTCCTGAGGT CAGGCCGTGA CTACTCAGGA GAGGAATGGA ATTCCAGGGC 2520
TCCTGCTCCT AATGAAGGAG AGGTGGGAGG GGCACACACC AAGCTGCTAC CAGGTACCAG 2580
GCCCTCGGAG GTGCTTGAAC ACTACCTCCT TGACTCTCAA TAGCAATCCT ATGAGGTGGA 2640
TGTTTTCTTG CCCAACAGAT GGGATTCTGA GACTCAGAGA TATTGGTGAC TTGCCCGAGG 2700
TCACACCAAT GGTAGGTGGT GATTCAAAAC CAGGTCTGTG TGCAGTTCAA TGACCATGGA 2760
GTCTTGCCCT GTTGCACAGG GCTTCTTGTG TCATACACAG CCTTCGCTTT GTGAAATCCA 2820
GCACAGTTGA CCCACATTCT CACCCAAATC CAAACTCCAA GTTTCAGAGC TTCTTTGCAC 2880
CCATAAAAGG GGGGCTCAGA AGTCCCCTTG AGGCCTCAGA AAGGACATAG ACCAAACAAA 2940
GGTTATGGCC TAATAAGAAG CAAATCAAAG TAACATTGCC TTATGATTTA AAAGTAGTAT 3000
GTGGGCCAGG TGCAGTGGCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGC 3050