EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-02779 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr1:201990770-201993060 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr1:201991522-201991537GAGGTCAGAAGTTCA+6.38
TBX21MA0690.1chr1:201992769-201992779AAGGTGTGAA+6.02
TBX2MA0688.1chr1:201992769-201992780AAGGTGTGAAT+6.02
ZNF263MA0528.1chr1:201992213-201992234CGCTCCTCCTCCTCCTCCTTC-8.44
ZNF263MA0528.1chr1:201992216-201992237TCCTCCTCCTCCTCCTTCTTC-8.69
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_23058chr1:201990827-201991297Colon_Crypt_1
SE_23058chr1:201991682-201993038Colon_Crypt_1
SE_23723chr1:201990919-201991273Colon_Crypt_2
SE_23723chr1:201991793-201992845Colon_Crypt_2
SE_24689chr1:201990748-201991252Colon_Crypt_3
SE_24689chr1:201991746-201993176Colon_Crypt_3
SE_25977chr1:201991449-201992586Duodenum_Smooth_Muscle
SE_26730chr1:201991584-201993071Esophagus
SE_27624chr1:201991445-201993333Fetal_Intestine
SE_28545chr1:201991443-201993383Fetal_Intestine_Large
SE_31432chr1:201991670-201993044Gastric
SE_33417chr1:201991427-201994657H2171
SE_33792chr1:201990657-201991281HCC1954
SE_33792chr1:201991430-201993180HCC1954
SE_34304chr1:201991505-201993289HCT-116
SE_34741chr1:201990653-201993194HeLa
SE_41626chr1:201991969-201992570LNCaP
SE_43434chr1:201990679-201991267MCF-7
SE_43434chr1:201991624-201993665MCF-7
SE_50066chr1:201991627-201993065Sigmoid_Colon
SE_52354chr1:201991432-201993050Small_Intestine
SE_56834chr1:201991684-201992300VACO_400
SE_56834chr1:201992323-201993032VACO_400
SE_57376chr1:201991848-201992311VACO_503
SE_57945chr1:201991851-201992344VACO_9m
SE_57945chr1:201992487-201992749VACO_9m
SE_65333chr1:201992691-201993394Pancreatic_islets
SE_67013chr1:201991427-201994657H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1201990800201992971
chr1201991192201991253
Enhancer Sequence
TCCACCTGGG CAACGAGAGC GAAATTCCGT CTCAAAAAAA AAAAAAAAAA TTTACTCCCT 60
ACATCATAAC TACCAGTGAT TTGTAGGACA GAGCACTCAA TGTAGAACAC TCTTCACTTT 120
GCAGATGAGG AAACTGAAGC TCAGAAAAGA AAGGTAACTT GCTCAAAGTC ACAAATCATG 180
TTGAATGGAG CCTGAGCTTC ATGTTGACAG CTGACCGCTT ACTGAGTATC TACTAGGTGC 240
CAGGCAATGT GTCAAGTTAT TGCTTTACAT ACATCATTCA TTCTCTCTGT GTTCATTAAC 300
TGTCTGCTGT GTGCATGGCT CCATGCTGTG TGCAGAAGAC CCAGTAGGGA AGAGGTCACC 360
CAGGGGGAGT AGGAAGCCTA GGCTATGGCC TGGCACGGTG GCTTATACCT GTAATCCCAG 420
CACTTTGGGA GGCTGAGGCG GGTAAATCAC CTGAGGGCAG GAATTTGAGA CCAGCCTGGC 480
CAACATGGCG AAACCCCATC TCTAGTAAAA ATACAAAAAT TAGCCGGGCG TGGTGGCGGG 540
TGCCTGTAAT CCCAGCTACT TTGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCGAGAGGA 600
GAAGGTTGCG GTGAGCCGAG ATCACACCAC TGCACTCCAG CCAGGCGACA GAGTGAGATT 660
CCATCTCAAA AAAAAAAAAA AAAAAAAATT CCTGGTGCAG TGGCTCAGGC TTGTAATCCC 720
AGCACTTTGG GAGGCTGAGG CGGATGAATC ATGAGGTCAG AAGTTCAAAA CCAGCCTGGC 780
CAAGATGGTG AAACCGCGTC TCTACTAAAA ATACAAAAAA ATTAGCCGGG TATGGTGGCA 840
GCTGCCTGTA ATACCAGCTA CTCGGAAGGC TGAGGCAGAT AATTGCTTGA ACCTGGGAGG 900
CAGAGGTTGC AGTGAGCTGA GATCATGCCA CTGCACTCCA GACTGGGTGG CAGAGTGAGA 960
CTCCATCTCA AAAAAAAAGA AAAGAAAAGA AAGAAAGCCT AGGCTAGAGC CTAGGAAATT 1020
CCAAAGACAT CTATATAAAC CTCTCAACAA GGTAGAGGAT AAGTGCCTCA TTTCACAGAT 1080
GAGCAAACTG AGGCTTCAGA GAGGTTAAGA AAAGCTTAAG CTCTCAGAGA TAGTAGTAAG 1140
TTTAGGAAAC CGGAGCTTGA ACCCTGCCTT CTTTCTTCAA TTCCACAGCT GACTCTGCTT 1200
TGAGAGGTGC TGAGCAACAC AAATGTCTCC GCTGTATGGG TGCCTAAAAC CCCACCATTA 1260
GATGTGCAGT TTGAGGAATG CCCTATGGAT ATACAAACAT GCCTGGGGTG GAGGGTGGAT 1320
TCAATGAGCA TTGCTTTCCA GGGACCCTTG GATCCTGCAG GGTGGATGGA AAGTGAGTTT 1380
TCAGTTCTTC AGAACCTCAC AGTGGCCAAC CCTTGGGAGC ATTGCCCTCT CATTCTTATC 1440
CTACGCTCCT CCTCCTCCTC CTTCTTCTGC TACGTGCAGG GCTGGGCTGG GGCACCAGCA 1500
GCAGCAATTA GCCCAGCTCA GCCGCCCGTT ACTGGAACCT GCATGTCAAC TCTGGAGCTG 1560
ATCCAAGAAA CCACACCCAG TGTCCTGCAT GACTCAACCT CACCTGCCCC CTCCACACCT 1620
GCCAGCCTCA GTGACCCAGG CCATAGTGCC CAGGGGAAAG TCCCAGCATC CTTTGGTCAA 1680
TCCTCATCTA CTCCATGTGT TTGTAAGGCC AGCTGGGATT TAGAGTCTTT GTATCACAGG 1740
CTTGATTCCG GGCTGATTTC TAGCCAGGAG AGAATGCTCC AGGCGGAGCA AATGCTGGGG 1800
TTTGGAAAAC TAGACTCTCC ATGGCAAATG CAGACAGATG GACCTCCTCT TCACTATCAT 1860
TGCTTGAAAC ACGAACAGCT TAAGGCCATG GGAGATATTA CTTTTCATAT GTCAAATTGG 1920
CAAAGAATTA AAGAATGCCC CTGATGTCTA GAGCTGGTGA GGATGTGAAG AAACTCAAAC 1980
TTGACAAAAA CCACTCGTCA AGGTGTGAAT TGAGAGACAC TTTTTTTTCG AGATGGAGTC 2040
TTGCGCTGTC GCCCACGCTG GAGTGTAGTG GTGCAATCTC AGCTCACTGC AACCTCTGCC 2100
TTCCAGATTC AAGCAGTGCT CCTGCCTCAG CCTCCCCAGT AGCTGGGACT ACAGGCACAC 2160
CACCACGCCC GGCTAATCCG CTTGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCATGA 2220
GCCACAGTGC CTGGCCGAGA GACATTTTCT TTCTTTTTAA TTTTTTAATG TTTATTTTTA 2280
TATATTTTTA 2290