EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-10454 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr14:35804560-35807580 
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
TTATTATGTT ATCATACACT AGATTTTATT GAATCTACCA TTTCACATTC TTATTGAGAG 60
TGTAACCTCT TGAAGCCTAC TGGTGCAGGA GGGATTTTGC AACCTTCCTT TGGCTTTTGT 120
CACCTATGGA AAACTACAAA CCAGCTTGCC TATCCGGTGA TTGGAACCAG GAGGATTGCC 180
GGCCTTGGGT CTGGAAATCC TATCCCATGT GTCTTCCTTC CTCCCTCCCT CCCTTCCTTG 240
GTTCCTTCCT TCCCCTGACT AGGCCCCAGA GGGGTGGGGA GGCCTTCCTG GGCCTGGCAT 300
CAGGGCTCCT GGGCTCCCAG CCAAGTGTCC AGAGGTCACT CCTCCTGGCA TCTGGATCCT 360
TCTTATCTTC CTGAGACATA GGAGGCTCCT GCTCTGGAGA TGACTGAAGG GAAAACACCT 420
GTATTTCCAG GGCCTTGGAA ATAGCCTGCT CCAGCCGGCC TTCCCGGGAG AAACTGAGAA 480
AGGACATTGG TCCGAAGCAT TTCTCTTTCG GTTTGTGCTG CGCTGAGCCT GTCCTGTGAT 540
GCGGCCCTCA CCAACCAAGG ACTGAACGAG AGGGACTCCA TGCGAACCTG CTCAGCATAC 600
AGCAGGTGCC TCGTGGATAT TCTTCCCTAA GGCTCCAGGC CAGCCAAGCA CTGCATTAAC 660
CAGGTTCGGA TGAACTTTAG AATGTACGCA TCTGAGCTGT CATAGTTTTT TGTTTTCTTG 720
TTTTTTTGAG ATGGAGTTTC GCTCTTTCAC CCAGGCTGGA GTGAAATGCC GCGATCTCAG 780
CTCACTGCAA CCTCTGCCTC CTGGGTTCAA GCCATTCTCC TGCCTCAGCC TCCCAAGTAT 840
CTGCGATTAC AGGCTCCTGC CACCATGTCC AGCTAATTTT TTGTATTTTT AGTAGAGACA 900
GGGTTTCACC ATGTTGGCCA GGCTGGTCTT GAATTCCTGA CCTCAGGTGA TCCACCCACC 960
TCGGCCTCCC AAAATGCTGG GATTACAGGC ATGAACCACT CTACCTGACC CATAGTTCTT 1020
AAATTTAAAA TCTTGATATG CTGGTGGATA TGCAGCTTGA TTTCTTTAAG CCGACATGGC 1080
CTGACTTTTT CAGATTCTCA GCCTGTGTTG GAGGGCTGTT GAGTGTTCTT TCTATGCAGA 1140
AAGTACGCCT GCCGTCCTCT GTTTTGTAAT CGCCACCCCA TCCCTGCCCA ACACACACAC 1200
CCACACAGCC GCAGTTACGC CGGGTCCAGC AACGCACGAA CCAAGTGGAA GGTCAAGGGC 1260
TGGGGCTCCG TTTCCCTCCC CTTGAAGCTG TTTGGTTTGC TCTTGTCCCA GCCCCTGACT 1320
GAGCCGCCAG CCCAGAACGG GGGCAGCCCT CCCCCATGCA GTCAGGGCCA GAGGAGCATA 1380
ATATTGCCCC CCCGGGTGCA GCCTTAGGTG CAGGAGCGTT GGGAATTTTC CATCTTGCTC 1440
TGCAGCCTGG CTTCTTAGGT CATCGTCCTG CTGCTGACAT AGGCCTGGGT TGGGCGAGTT 1500
TCCTGCAGGT CAGCGAGGGC GCGGAGGCAG CGCCTGAGCC TGCTCAGGGC CTGGCTTCCT 1560
GCCTGCTGTG AGGAAGGGTG GAGGAGGGGT TCGAGGCCTC AACCATCCCT TGGCCCAGAG 1620
CCTCAGGCCA AGCAGCCTCC GCCTCTGCCC AGGCCTGTCT CCTCCCGGCC TCCTGCTCTC 1680
CTGTTTCCTA AAGCTTTCCC GCTGGGTGGC TCCCAGTTCT TCCAGAAATC CCCTCCAGGA 1740
AATTTGCTTG TTGCCACAAA ATAATGCAAA TCTGTTCCTG GGGCCGCCCA GGCAACCTGC 1800
AGTCTCTGTC TCCCCAAGAC CTGAGGAGGG AGGGCGAGGC AGGCCCTGTG CCCGTCAGGG 1860
TCCCTTTTCC AGCCATGAGG ACAAAGGATA AGCCGCACCC TCGTCACCCT CTCATAAGCT 1920
GCAAGAGAAA GTTCCTGGTT TTACCTCTAA GGGAACCAGC TCCACCTAGG GAAAGGCCAC 1980
ACAGGACCCT CAAAGGCACC AAGGTCTTTT TTCTATTTAA TATCTAAAAC AGTCTGAATA 2040
TATTAAAGTT TATGCTCATG TTTGGCATTT GTTTATCTGT TTCTCGAACT TCAACTCCCT 2100
GCCGTGTCTG GAGCAGAAAG TGAAGGCCCA TGGATAACAC TTCTGCGTGC CACAGTCCTA 2160
GGTGGTGACC AATGCAGGGA TGCACAGGTG CCGTGTGGCC TTCTGCAGGC CAGGCCCCAC 2220
AGAGACCCAC AGTCAAGGTG GCCTGAGACC CTTGAACAAG GAGCTTGTGG CCAGAGAAAG 2280
GCTAAATGCA GCACCCCCAC CCCTGTGGCT AGTGCCAGGG CCCCACCTGA ATGCTCTGCA 2340
GTTGGGTCCC CCCAGGCCAT CTCCAGAGGA GAACGCAAGT GGGCTAGGGA GGGAACAGAC 2400
CAGCCTGATG CAAAACCCTC TCAGCCCAGC ACAGCCCTCG TGTCCCTGGG CTGAGGGTCT 2460
GGGGAGAACA TCACTTGCTC TTGCCTCCCT TCCTTTCTTG CTGCTGCTGC CTCCTGAGGT 2520
CAGGCCGTGA CTACTCAGGA GAGGAATGGA ATTCCAGGGC TCCTGCTCCT AATGAAGGAG 2580
AGGTGGGAGG GGCACACACC AAGCTGCTAC CAGGTACCAG GCCCTCGGAG GTGCTTGAAC 2640
ACTACCTCCT TGACTCTCAA TAGCAATCCT ATGAGGTGGA TGTTTTCTTG CCCAACAGAT 2700
GGGATTCTGA GACTCAGAGA TATTGGTGAC TTGCCCGAGG TCACACCAAT GGTAGGTGGT 2760
GATTCAAAAC CAGGTCTGTG TGCAGTTCAA TGACCATGGA GTCTTGCCCT GTTGCACAGG 2820
GCTTCTTGTG TCATACACAG CCTTCGCTTT GTGAAATCCA GCACAGTTGA CCCACATTCT 2880
CACCCAAATC CAAACTCCAA GTTTCAGAGC TTCTTTGCAC CCATAAAAGG GGGGCTCAGA 2940
AGTCCCCTTG AGGCCTCAGA AAGGACATAG ACCAAACAAA GGTTATGGCC TAATAAGAAG 3000
CAAATCAAAG TAACATTGCC 3020