| Tag | Content |
|---|
EnhancerAtlas ID | HS161-01388 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr1:201990470-201993190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:201991522-201991537 | GAGGTCAGAAGTTCA | + | 6.38 | | TBX21 | MA0690.1 | chr1:201992769-201992779 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr1:201992769-201992780 | AAGGTGTGAAT | + | 6.02 | | ZNF263 | MA0528.1 | chr1:201992213-201992234 | CGCTCCTCCTCCTCCTCCTTC | - | 8.44 | | ZNF263 | MA0528.1 | chr1:201992216-201992237 | TCCTCCTCCTCCTCCTTCTTC | - | 8.69 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_23058 | chr1:201990827-201991297 | Colon_Crypt_1 | | SE_23058 | chr1:201991682-201993038 | Colon_Crypt_1 | | SE_23723 | chr1:201990919-201991273 | Colon_Crypt_2 | | SE_23723 | chr1:201991793-201992845 | Colon_Crypt_2 | | SE_24689 | chr1:201990748-201991252 | Colon_Crypt_3 | | SE_24689 | chr1:201991746-201993176 | Colon_Crypt_3 | | SE_25977 | chr1:201991449-201992586 | Duodenum_Smooth_Muscle | | SE_26730 | chr1:201991584-201993071 | Esophagus | | SE_27624 | chr1:201991445-201993333 | Fetal_Intestine | | SE_28545 | chr1:201991443-201993383 | Fetal_Intestine_Large | | SE_31432 | chr1:201991670-201993044 | Gastric | | SE_33417 | chr1:201991427-201994657 | H2171 | | SE_33792 | chr1:201990657-201991281 | HCC1954 | | SE_33792 | chr1:201991430-201993180 | HCC1954 | | SE_34304 | chr1:201991505-201993289 | HCT-116 | | SE_34741 | chr1:201990653-201993194 | HeLa | | SE_41626 | chr1:201991969-201992570 | LNCaP | | SE_43434 | chr1:201990679-201991267 | MCF-7 | | SE_43434 | chr1:201991624-201993665 | MCF-7 | | SE_50066 | chr1:201991627-201993065 | Sigmoid_Colon | | SE_52354 | chr1:201991432-201993050 | Small_Intestine | | SE_56834 | chr1:201991684-201992300 | VACO_400 | | SE_56834 | chr1:201992323-201993032 | VACO_400 | | SE_57376 | chr1:201991848-201992311 | VACO_503 | | SE_57945 | chr1:201991851-201992344 | VACO_9m | | SE_65333 | chr1:201992691-201993394 | Pancreatic_islets | | SE_67013 | chr1:201991427-201994657 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 201990800 | 201992971 | | chr1 | 201991192 | 201991253 |
|
Enhancer Sequence | TCAACCCATC TCTTTTCAGG AAGAACAAGC ACCTTAAATT AGTCCTTACA TCGGCCAAGT 60
GCAGTGGCTC ATGCCTGTAA TCCCAGCACT TTGGGAGACA GAGGCAGGCG GATCACCTGA 120
GGTCGGGAGT TCGAGACCAG CCTGACCAAC ATGGAAAAAC CCTGTCTCTA CTAAAAACAC 180
AAAATTACCC AGGCGTCGTG GTGCATACCT GTAGTCCCAG CTACTTGGGA GGCTGAGGCA 240
GGAGAATCGC TTGAACCTGG GAGGCAGAGG TTGCAATGAG CCGAGATCAC GCCATTGCAC 300
TCCACCTGGG CAACGAGAGC GAAATTCCGT CTCAAAAAAA AAAAAAAAAA TTTACTCCCT 360
ACATCATAAC TACCAGTGAT TTGTAGGACA GAGCACTCAA TGTAGAACAC TCTTCACTTT 420
GCAGATGAGG AAACTGAAGC TCAGAAAAGA AAGGTAACTT GCTCAAAGTC ACAAATCATG 480
TTGAATGGAG CCTGAGCTTC ATGTTGACAG CTGACCGCTT ACTGAGTATC TACTAGGTGC 540
CAGGCAATGT GTCAAGTTAT TGCTTTACAT ACATCATTCA TTCTCTCTGT GTTCATTAAC 600
TGTCTGCTGT GTGCATGGCT CCATGCTGTG TGCAGAAGAC CCAGTAGGGA AGAGGTCACC 660
CAGGGGGAGT AGGAAGCCTA GGCTATGGCC TGGCACGGTG GCTTATACCT GTAATCCCAG 720
CACTTTGGGA GGCTGAGGCG GGTAAATCAC CTGAGGGCAG GAATTTGAGA CCAGCCTGGC 780
CAACATGGCG AAACCCCATC TCTAGTAAAA ATACAAAAAT TAGCCGGGCG TGGTGGCGGG 840
TGCCTGTAAT CCCAGCTACT TTGGAGGCTG AGGCAGGAGA ATCACTTGAA CCCGAGAGGA 900
GAAGGTTGCG GTGAGCCGAG ATCACACCAC TGCACTCCAG CCAGGCGACA GAGTGAGATT 960
CCATCTCAAA AAAAAAAAAA AAAAAAAATT CCTGGTGCAG TGGCTCAGGC TTGTAATCCC 1020
AGCACTTTGG GAGGCTGAGG CGGATGAATC ATGAGGTCAG AAGTTCAAAA CCAGCCTGGC 1080
CAAGATGGTG AAACCGCGTC TCTACTAAAA ATACAAAAAA ATTAGCCGGG TATGGTGGCA 1140
GCTGCCTGTA ATACCAGCTA CTCGGAAGGC TGAGGCAGAT AATTGCTTGA ACCTGGGAGG 1200
CAGAGGTTGC AGTGAGCTGA GATCATGCCA CTGCACTCCA GACTGGGTGG CAGAGTGAGA 1260
CTCCATCTCA AAAAAAAAGA AAAGAAAAGA AAGAAAGCCT AGGCTAGAGC CTAGGAAATT 1320
CCAAAGACAT CTATATAAAC CTCTCAACAA GGTAGAGGAT AAGTGCCTCA TTTCACAGAT 1380
GAGCAAACTG AGGCTTCAGA GAGGTTAAGA AAAGCTTAAG CTCTCAGAGA TAGTAGTAAG 1440
TTTAGGAAAC CGGAGCTTGA ACCCTGCCTT CTTTCTTCAA TTCCACAGCT GACTCTGCTT 1500
TGAGAGGTGC TGAGCAACAC AAATGTCTCC GCTGTATGGG TGCCTAAAAC CCCACCATTA 1560
GATGTGCAGT TTGAGGAATG CCCTATGGAT ATACAAACAT GCCTGGGGTG GAGGGTGGAT 1620
TCAATGAGCA TTGCTTTCCA GGGACCCTTG GATCCTGCAG GGTGGATGGA AAGTGAGTTT 1680
TCAGTTCTTC AGAACCTCAC AGTGGCCAAC CCTTGGGAGC ATTGCCCTCT CATTCTTATC 1740
CTACGCTCCT CCTCCTCCTC CTTCTTCTGC TACGTGCAGG GCTGGGCTGG GGCACCAGCA 1800
GCAGCAATTA GCCCAGCTCA GCCGCCCGTT ACTGGAACCT GCATGTCAAC TCTGGAGCTG 1860
ATCCAAGAAA CCACACCCAG TGTCCTGCAT GACTCAACCT CACCTGCCCC CTCCACACCT 1920
GCCAGCCTCA GTGACCCAGG CCATAGTGCC CAGGGGAAAG TCCCAGCATC CTTTGGTCAA 1980
TCCTCATCTA CTCCATGTGT TTGTAAGGCC AGCTGGGATT TAGAGTCTTT GTATCACAGG 2040
CTTGATTCCG GGCTGATTTC TAGCCAGGAG AGAATGCTCC AGGCGGAGCA AATGCTGGGG 2100
TTTGGAAAAC TAGACTCTCC ATGGCAAATG CAGACAGATG GACCTCCTCT TCACTATCAT 2160
TGCTTGAAAC ACGAACAGCT TAAGGCCATG GGAGATATTA CTTTTCATAT GTCAAATTGG 2220
CAAAGAATTA AAGAATGCCC CTGATGTCTA GAGCTGGTGA GGATGTGAAG AAACTCAAAC 2280
TTGACAAAAA CCACTCGTCA AGGTGTGAAT TGAGAGACAC TTTTTTTTCG AGATGGAGTC 2340
TTGCGCTGTC GCCCACGCTG GAGTGTAGTG GTGCAATCTC AGCTCACTGC AACCTCTGCC 2400
TTCCAGATTC AAGCAGTGCT CCTGCCTCAG CCTCCCCAGT AGCTGGGACT ACAGGCACAC 2460
CACCACGCCC GGCTAATCCG CTTGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCATGA 2520
GCCACAGTGC CTGGCCGAGA GACATTTTCT TTCTTTTTAA TTTTTTAATG TTTATTTTTA 2580
TATATTTTTA AACTTTTTTT TTTTTTGAGA TAGGGTCTTA CTCTATCACC TAGGCTGGAG 2640
TGCAGTGGCA TGATCATGGC TCACTGTAGC CTTGAGCCTC CCCCACCCCC AGGGCCCAAG 2700
TGATCCTCCC ATCTCAGCCT 2720
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