EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS129-02919 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr1:201990750-201993250 
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
CCGAGATCAC GCCATTGCAC TCCACCTGGG CAACGAGAGC GAAATTCCGT CTCAAAAAAA 60
AAAAAAAAAA TTTACTCCCT ACATCATAAC TACCAGTGAT TTGTAGGACA GAGCACTCAA 120
TGTAGAACAC TCTTCACTTT GCAGATGAGG AAACTGAAGC TCAGAAAAGA AAGGTAACTT 180
GCTCAAAGTC ACAAATCATG TTGAATGGAG CCTGAGCTTC ATGTTGACAG CTGACCGCTT 240
ACTGAGTATC TACTAGGTGC CAGGCAATGT GTCAAGTTAT TGCTTTACAT ACATCATTCA 300
TTCTCTCTGT GTTCATTAAC TGTCTGCTGT GTGCATGGCT CCATGCTGTG TGCAGAAGAC 360
CCAGTAGGGA AGAGGTCACC CAGGGGGAGT AGGAAGCCTA GGCTATGGCC TGGCACGGTG 420
GCTTATACCT GTAATCCCAG CACTTTGGGA GGCTGAGGCG GGTAAATCAC CTGAGGGCAG 480
GAATTTGAGA CCAGCCTGGC CAACATGGCG AAACCCCATC TCTAGTAAAA ATACAAAAAT 540
TAGCCGGGCG TGGTGGCGGG TGCCTGTAAT CCCAGCTACT TTGGAGGCTG AGGCAGGAGA 600
ATCACTTGAA CCCGAGAGGA GAAGGTTGCG GTGAGCCGAG ATCACACCAC TGCACTCCAG 660
CCAGGCGACA GAGTGAGATT CCATCTCAAA AAAAAAAAAA AAAAAAAATT CCTGGTGCAG 720
TGGCTCAGGC TTGTAATCCC AGCACTTTGG GAGGCTGAGG CGGATGAATC ATGAGGTCAG 780
AAGTTCAAAA CCAGCCTGGC CAAGATGGTG AAACCGCGTC TCTACTAAAA ATACAAAAAA 840
ATTAGCCGGG TATGGTGGCA GCTGCCTGTA ATACCAGCTA CTCGGAAGGC TGAGGCAGAT 900
AATTGCTTGA ACCTGGGAGG CAGAGGTTGC AGTGAGCTGA GATCATGCCA CTGCACTCCA 960
GACTGGGTGG CAGAGTGAGA CTCCATCTCA AAAAAAAAGA AAAGAAAAGA AAGAAAGCCT 1020
AGGCTAGAGC CTAGGAAATT CCAAAGACAT CTATATAAAC CTCTCAACAA GGTAGAGGAT 1080
AAGTGCCTCA TTTCACAGAT GAGCAAACTG AGGCTTCAGA GAGGTTAAGA AAAGCTTAAG 1140
CTCTCAGAGA TAGTAGTAAG TTTAGGAAAC CGGAGCTTGA ACCCTGCCTT CTTTCTTCAA 1200
TTCCACAGCT GACTCTGCTT TGAGAGGTGC TGAGCAACAC AAATGTCTCC GCTGTATGGG 1260
TGCCTAAAAC CCCACCATTA GATGTGCAGT TTGAGGAATG CCCTATGGAT ATACAAACAT 1320
GCCTGGGGTG GAGGGTGGAT TCAATGAGCA TTGCTTTCCA GGGACCCTTG GATCCTGCAG 1380
GGTGGATGGA AAGTGAGTTT TCAGTTCTTC AGAACCTCAC AGTGGCCAAC CCTTGGGAGC 1440
ATTGCCCTCT CATTCTTATC CTACGCTCCT CCTCCTCCTC CTTCTTCTGC TACGTGCAGG 1500
GCTGGGCTGG GGCACCAGCA GCAGCAATTA GCCCAGCTCA GCCGCCCGTT ACTGGAACCT 1560
GCATGTCAAC TCTGGAGCTG ATCCAAGAAA CCACACCCAG TGTCCTGCAT GACTCAACCT 1620
CACCTGCCCC CTCCACACCT GCCAGCCTCA GTGACCCAGG CCATAGTGCC CAGGGGAAAG 1680
TCCCAGCATC CTTTGGTCAA TCCTCATCTA CTCCATGTGT TTGTAAGGCC AGCTGGGATT 1740
TAGAGTCTTT GTATCACAGG CTTGATTCCG GGCTGATTTC TAGCCAGGAG AGAATGCTCC 1800
AGGCGGAGCA AATGCTGGGG TTTGGAAAAC TAGACTCTCC ATGGCAAATG CAGACAGATG 1860
GACCTCCTCT TCACTATCAT TGCTTGAAAC ACGAACAGCT TAAGGCCATG GGAGATATTA 1920
CTTTTCATAT GTCAAATTGG CAAAGAATTA AAGAATGCCC CTGATGTCTA GAGCTGGTGA 1980
GGATGTGAAG AAACTCAAAC TTGACAAAAA CCACTCGTCA AGGTGTGAAT TGAGAGACAC 2040
TTTTTTTTCG AGATGGAGTC TTGCGCTGTC GCCCACGCTG GAGTGTAGTG GTGCAATCTC 2100
AGCTCACTGC AACCTCTGCC TTCCAGATTC AAGCAGTGCT CCTGCCTCAG CCTCCCCAGT 2160
AGCTGGGACT ACAGGCACAC CACCACGCCC GGCTAATCCG CTTGCCTTGG CCTCCCAAAG 2220
TGCTGGGATT ACAGGCATGA GCCACAGTGC CTGGCCGAGA GACATTTTCT TTCTTTTTAA 2280
TTTTTTAATG TTTATTTTTA TATATTTTTA AACTTTTTTT TTTTTTGAGA TAGGGTCTTA 2340
CTCTATCACC TAGGCTGGAG TGCAGTGGCA TGATCATGGC TCACTGTAGC CTTGAGCCTC 2400
CCCCACCCCC AGGGCCCAAG TGATCCTCCC ATCTCAGCCT CCCAAGTAGT TGGGACCGCA 2460
GTCATGTGCC ACCGCACCCA GCTAATTTTT TAATTTAATT 2500