EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-27607 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr20:48982250-48987330 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6067417chr2048983697hg19
TF binding sites/motifs
Number: 25             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr20:48983073-48983091CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983077-48983095CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983081-48983099CCTTCCTTCCTTCCTTCC-10.83
EWSR1-FLI1MA0149.1chr20:48983061-48983079CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr20:48983043-48983061CCCTCCCTCCCTCCTTCC-7.12
EWSR1-FLI1MA0149.1chr20:48983085-48983103CCTTCCTTCCTTCCTTTT-7.95
EWSR1-FLI1MA0149.1chr20:48983065-48983083CCTCCCTCCCTTCCTTCC-8.13
EWSR1-FLI1MA0149.1chr20:48983069-48983087CCTCCCTTCCTTCCTTCC-9.42
FOXA1MA0148.4chr20:48982288-48982304TATTGTTTGCTTAATG-6.2
IRF1MA0050.2chr20:48983319-48983340ACACAGTTTCATTTTCACCTT+6.64
MyogMA0500.1chr20:48984003-48984014GACAGCTGCTG+6.14
Stat6MA0520.1chr20:48983524-48983539GTTTTCCAGAGAAAA+6.07
Tcf12MA0521.1chr20:48984003-48984014GACAGCTGCTG+6.02
ZNF263MA0528.1chr20:48983056-48983077CTTCCCCTCCCTCCCTCCCTT-6.14
ZNF263MA0528.1chr20:48983081-48983102CCTTCCTTCCTTCCTTCCTTT-6.16
ZNF263MA0528.1chr20:48983043-48983064CCCTCCCTCCCTCCTTCCCCT-6.46
ZNF263MA0528.1chr20:48983042-48983063TCCCTCCCTCCCTCCTTCCCC-6.61
ZNF263MA0528.1chr20:48983069-48983090CCTCCCTTCCTTCCTTCCTTC-6.76
ZNF263MA0528.1chr20:48983073-48983094CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr20:48983077-48983098CCTTCCTTCCTTCCTTCCTTC-6.94
ZNF263MA0528.1chr20:48983039-48983060GTCTCCCTCCCTCCCTCCTTC-7.12
ZNF263MA0528.1chr20:48983065-48983086CCTCCCTCCCTTCCTTCCTTC-7.19
ZNF263MA0528.1chr20:48983061-48983082CCTCCCTCCCTCCCTTCCTTC-7.38
ZNF263MA0528.1chr20:48983052-48983073CCTCCTTCCCCTCCCTCCCTC-7.65
ZNF263MA0528.1chr20:48983048-48983069CCTCCCTCCTTCCCCTCCCTC-7.73
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_28491chr20:48982335-48987321Fetal_Intestine
SE_31629chr20:48983043-48983874Gastric
SE_31629chr20:48985416-48986768Gastric
SE_33764chr20:48982789-48984100HCC1954
SE_42215chr20:48984303-48987016Lung
SE_52401chr20:48982681-48987083Small_Intestine
SE_53316chr20:48982599-48984069Spleen
SE_56118chr20:48982851-48984157u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr204898308348983800
Number: 1             
IDChromosomeStartEnd
GH20I050365chr204898243148987174
Enhancer Sequence
TCATAAATTT TTAATACAGC ATTTCATTAT ATGAGGACTA TTGTTTGCTT AATGAATCTT 60
CTGTAGTTTG GCATTTCAGA ATTTTTTCCC CCAATTTTTC ACTATTATAA ACAATGCTGC 120
AATGAACGAC CTTCCCCGTA GAGACTACTT GGCCTATTAG AATAAATGCC CCCAAGTTAA 180
ATTTCCAGGT TGCTTTAAAA TTTCTGCCCA GTGAACAGCA TGGTGCTTGT TGCCATTCTG 240
CTCCCAGAGA CCCTTGTAGA GTCCGTTCGG GACAGTATGA GAATCCCCAT TATCCCATAC 300
TCTGCAACAC TGAGAGTTGC CAATCTTTTT TGTCTTTTCT AATCTGATAG GCAGAAAATG 360
ACATATCATT GTAGCTTATC ATTGATAACT GGTGGGGTGG AACTTGTCTT CATACTTTTT 420
TTTCTTTTTT TCTGAGGCAG TGTCTCCCTT TGTCTCCCAG GCTGGAGTGC AGTGGCACCA 480
TCTCAGCTCC TACATCAGCC TCCCAAGTAG CTGGGACTAC AGGCATATGC CACCACACCT 540
GTCTAATTTT CCTTATTTTT TGTAGAGATG AGATCTTTCT GTGTTACCCA GGCTGGTCTT 600
AAACTCCTGG GCTCAAGCAA TCCTTCCACC TCGGCCTCCC AAAGTGCTGG GATTATAGGC 660
ATGAGCTGCC TCGCCTGCCA GAATAGTGGG TTTTTAATAC GGTGTTTACC TCTTCTTATT 720
GTTTTGCAAG AACTCTTTGT ATATTAAGGA TAGTAATTCT TTCTAAGAGT CTTATAATTG 780
ACTATAAAAG TCTCCCTCCC TCCCTCCTTC CCCTCCCTCC CTCCCTTCCT TCCTTCCTTC 840
CTTCCTTCCT TTTGTTCCCT TCTGCTTTCT AAGGATATGC CTGGTGTTTG GCAAGCATTG 900
CATGAATTAC ATTAGGAAAT AACTTTTGTA ACAAACCCAT TTAACAACCA TTCTTTGTTC 960
CCCGCCTCCT GATAATGCTC AGAGCCACAG CAACAGCCTT TGCCCAACTC CATGTCATTA 1020
ACCCTTGATC TTTTCCTGCT GAATAGCAGA TTGCTTTCCG GGGCTGGCAA CACAGTTTCA 1080
TTTTCACCTT CCTGCTGATG GAACTGCCCT GGCTCTGTGC CAGATGGCTG TTTACATAAG 1140
AAATGATTTG ATTATATTGC ACAGCCAATG GCAGCCTTTC TCAGAATAAA GAAGCCAGAA 1200
ACATATAATC AAAGCCATTA ACTGTGTACA AAGAAACGCA GCCCACTCTA AATTTCCCAC 1260
CAACCATAAT CACAGTTTTC CAGAGAAAAA TAAGAACAGG GTTATGGTTC CCTACTAAAA 1320
ACGTGTTAGG GGAAAGACTT TTAAAAGGAA ATTGTGGTAT AGCTCAGTTG CACTCTCAGA 1380
TCAACCCTTG AGCCTTGACT CCAATCCCAG CTCTGTAACT CACTGTCCTT GTGACCTTGG 1440
AAAAGTCGTT TACTGCCAAA AGCCTCCGTT TCTTTATTGT AAAATGGCTA TAATAGTAAT 1500
ATCAACCTCA GAGGTTTACG AGAGGATTAA GTGAGATAGT GCATAAGAAC ACTTTCTCAG 1560
TCAGAATGTT TTCAGCCGCA AGGAGCAGAA CACTTGACTA AAGGAGGGAA AAAAAAGCTA 1620
GAGGACTTAT AATTTTATTT AACAGGGTTG TTTCATTTGG AGGCATAAAG ATGTAACCAG 1680
TGATTCACAT TCTTTTCTTC TTCCTGCTAT GCCATTCTCA GCAATTTATG GACATGTCTC 1740
CTCATGGTTT CAAGACAGCT GCTGTGGCTC CAGGCATCAC ACTGGGACAT GATAAAATCA 1800
AGCAAAGAGG AGGAGGGCAT TTTTTCCCCT GTGTCTCCTT TCATGATGGA GAAAATTGTT 1860
CCCAAATTTC CCCCCTGCAG ATCTGCAGAC TTCTTATTGG CCAAGATGGC GTTACATCTA 1920
TAATTCCAAA CCAGTCACTG ATGGAGGAAT GAGAATGACT GCAGTTGGCT TGGACCTATA 1980
ACTCACTCTG AAGCCGGGGC GAGGAATAGC CACCGTCCCT GAGCTCCTGA GTAGATGCAC 2040
AACCAACAAA ACTGAATCCC GTCAGCGAAG GAGTCATGGG TGGGCAACCC GTGCTGTGTC 2100
TACCATAAGC ACAACTCCTG GTGCTCATGA GGTGCCCCCA AAGGCTGGCA TTTGGCAAGC 2160
TCAAGACTGG GAGTCCACAC AGTGCTCCAG GTGGGAGGAT CACAACCGCG ATTGGCCAGG 2220
GAGTCCCTCT GGGTGCCAGA CCCCTGTATG CAAAGCCCCA CTCAGCATCT CCACTTGATT 2280
GGCTTATGGG AACCTCAAAT CCAACACACT ATATTTGAAC TCATCATATT TCCTCCCCAC 2340
TGGCCTCCTC TGTTGGTACC CACCTTGCTC AAGCCAGAAG CTGGCTGGTC CTCAGGAGTC 2400
CCTGCTTTCC TTCCCCATCT GTGCCCACGT CTCTCCAGCT CTGCCATCAT CTTCCACCTG 2460
GACACCAACC AAGCCCCCGC TCTCCCTGCT GCTGTGTGGG CATCAACAGC CTATGCTGTT 2520
CCCTCTGAAC GGAACTCTTC CCGCTCCTGT TTCCCTGTCA CCTTGCTCAG GAAAGCTCTT 2580
CTGATCCCCC CAAGTTGAAT CCCTCATTAC AAACCTCACA TCCTGACATA CATCTCTCCA 2640
TTGCCCTGAT CATACTTCTT ATTTACCTGT GTGATTATTT CACTCATGTC TCACCCCACC 2700
AGGTTGCAGC TCCATGAGGG TGGGAATTGG GTCTGTTTTG TTCACTGATA ACCTTCAGTG 2760
CCTGACACAT AGTAGGGCCT CAATTTTATT CCTGAATCCC ATAAATGAAT AAATTCATCC 2820
CCTGCCCTGT GGCCAGGGAG ATCACTCTAA GAAGCAAATC TAATCACTCC CTCTCCTGCC 2880
ATAAGCCTTC CATGGCTCCC CTTTACCCAC AGGACAAAGT CTAAAGGGCT TAACCTGGCT 2940
CTTTCAGGCT CCTCAAAGTG GATTCTGCCA CCTCTCCAGC CCCATCTCAC CTGCCCCATT 3000
GTCCTTTACG GTCCAGCCAC CCTCTACTCC TTTAGGTGTC TCAAAGTCTG CATGTTCTCT 3060
CCTATCCCTG GATTTGCCTA TATGCTATGT TTCTCCCGGA AACTTTGTCT CAAAAAATCT 3120
TCATTCTCAT TGCCAAGGCT TTAAAATTTG CCTCTTTTGG GGAAGGTTTA GTTCTGTAAG 3180
CTCATTCTGG AAATCTGGGT TCCTTCTATC TAGCTGTTGT CATCCTCAGT CCATAGCTTC 3240
CAGTCAAGTC CAAAACAGCT GCTATAGCTT CTCCGTCACA TCTACGTTCC AGGCAGTGGG 3300
GAGAGAGAAA GGGTCATTCC TCTTAAGGGC ATGACTCAGA AGCAGTGCTA TCACTTCTAC 3360
TCAATCCCAT TGGCTGGAGC TCAGTCATAT GACCATGCCT AACTGCAAAG GAGGCCGGGA 3420
AATAGAATCA CTATCTGCCG ATTATGTTAG CATGTTTCCC ACTAATGCTC CAAAATTCTC 3480
TCAGTATGAG AAAAAAGCTG ATGGATGTTG GTGGACACTG ATGGTCCTGC CACACTCACC 3540
CCCACAGTGC CAGTCATGGA CTTATCTCTG CCCAGCCAGA CTGTGAGCTC CCTAAGGACA 3600
GGGACCATAT ATGGTGGTCA TTGCAGCATC CCCTGCAACT CACAGAGTGC TGGTTGTGAC 3660
ATATGGCAAA TCAGAGTGAA TTGCAGAGGC CGGAAATACA AGGTGGAGAA ACTGAGGCAG 3720
GCACCAGTTG AGTTCCACAC ACATTTTCTG GGTGCTGATT ACACATAAGA ACCCTGGGCT 3780
TGGTCCCGGT GCCTGGGGGG CAGCAACACT TGTCTGGCCT GGCAGTGTCC CCAAAAGCAC 3840
CCAGTTGGGG GCTGCAAGGC CCCACCCGGT GGGGAAGCTG CAGAAACAGA GCAGAGTCCA 3900
CAGTCAGAAC AGGAGGCGCC ACAAGGGCCT ACAGGTAAGG CAGGTCCCAG GCCCTCAGCC 3960
CACCTGGCCC TGGCCCTGCT GCACTCTTGG CCACTCCCCA ACATTATCTG GCCTTGGGCC 4020
CAGCCCTGAG CACCTGCCCT TCCCTGCTCT CCCGAGAGGC CTGAGCTGGG GTTCCCCTCC 4080
CCTGTCGGCT GCCGTGGGAA AGGCCTTATG GTAGCTCTCA AGGTCCAAGT TCCAGCCTCA 4140
ACAGCTGCCG TACTTGCTAT TCCCTCTGGC CAGACCTCCC TTCCGTGCTG CTCTAGCTTC 4200
TCCTGCTCTC AGCTTAGACG GCACCTCCTC ACTGTCTCCA AAGACCACCG CCCACCCCGG 4260
TGCCTCTCCA CCACATTGTG CATCTTGTTG CTTCCCAGCA TGGGTCTGTG TGGGGTCGTA 4320
GGGGAATCCT GCTCTTGTTC ATTCATTTGT TGGCTTCTTT GCTCGCTGTC TCCCCCAGTA 4380
GAGACATGGA CATTTTCTGT CTTGTTTTCC ACTGTATCCA GAGCCTAGCC CAGGGCCTGG 4440
CACCTAGTAG GTGTTCAGGT AATATCTATG GACTACCTAC ATACACACAC AGTGAGGAAA 4500
GACAAGAGAA TTAGCACTCA CTGCACTCGT ATGACATGCC AGCGCATGCG TTGTTCACTC 4560
TGAGGCCCAC GACATCATTG CCTGGTTGGA ATCATTATCT CCATTTCACA GTGGAGGAAA 4620
CTGAGACTCA GAGAAATGAA GTGACTCGAC CGAGGTTACG CCAATAGGAA GGGCCAAGTC 4680
TCAGACGGGG GGGGATATTT ATAACGAAAT GCAAAGATCT TGGAGGAGGG GGTGGATTCT 4740
TGGTTGTACA CATCGATCAA AGCTCATCAA ACTGTACAGT TGAAATCAGA GGTTCTCAAC 4800
CAAGCATGGT TTTACCCCCA GGAGACATTC AGCAAAGTGC AGAGACATTT GGTCATCATG 4860
GGGGTAAGCA ATGCTACTGG CATCTCGTGG GTAGAGGCCA GAGATGCCGC TCAACATCCT 4920
ACAGTGCCCA GGACAGCCGC CACAGCAAAG AATTATCTGA CCCAAAATGT CAGTAGTGCT 4980
AGGTTGAGAA ACTCTGCTTT GAAGGAATGT AGTTTACTGA ACACAAATTA TGTACTCCAT 5040
TTATTAAGGC ATAATCAATG CATTTTTTGT AAAATAGAAA 5080