| Tag | Content |
|---|
EnhancerAtlas ID | HS161-06847 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr17:48765610-48768450 |
Target genes | | Number: 27 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr17:48766766-48766777 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr17:48766766-48766777 | GGGTGACTCAG | + | 6.02 | | Stat6 | MA0520.1 | chr17:48765708-48765723 | CACTTCCTAAGAAAC | + | 6.18 | | TFAP2C | MA0524.2 | chr17:48767512-48767524 | TGCCCCAAGGCA | + | 6.62 | | ZNF263 | MA0528.1 | chr17:48766834-48766855 | AGGGGAGGAGGAGGCAGGAGG | + | 6.48 |
|
| | Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
| SE_01111 | chr17:48763013-48766174 | Adrenal_Gland | | SE_01111 | chr17:48766213-48768739 | Adrenal_Gland | | SE_23407 | chr17:48765541-48766036 | Colon_Crypt_1 | | SE_23407 | chr17:48766365-48771239 | Colon_Crypt_1 | | SE_24075 | chr17:48765520-48766009 | Colon_Crypt_2 | | SE_24075 | chr17:48766497-48768886 | Colon_Crypt_2 | | SE_27993 | chr17:48760869-48773354 | Fetal_Intestine | | SE_28941 | chr17:48761067-48773571 | Fetal_Intestine_Large | | SE_31702 | chr17:48766549-48772059 | Gastric | | SE_34102 | chr17:48766527-48771339 | HCC1954 | | SE_34277 | chr17:48760595-48768866 | HCT-116 | | SE_34841 | chr17:48766371-48767399 | HeLa | | SE_47221 | chr17:48766440-48773537 | Panc1 | | SE_47987 | chr17:48766691-48767251 | Pancreas | | SE_47987 | chr17:48767352-48768845 | Pancreas | | SE_50493 | chr17:48766391-48771333 | Sigmoid_Colon | | SE_53061 | chr17:48760980-48766139 | Small_Intestine | | SE_53061 | chr17:48766385-48771338 | Small_Intestine | | SE_65786 | chr17:48766280-48768596 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 48765795 | 48765962 | | chr17 | 48767377 | 48767800 | | chr17 | 48767800 | 48768400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I050683 | chr17 | 48760941 | 48774865 |
|
Enhancer Sequence | GGGCTCCACA GGCACTGTCT TTGTGCACAG GCCACTTGCA TCCTGCCTCC TCCATGAGGC 60
AATGTAAGGG GAACTGGAGG CTTCATGCTG AGTCCCATCA CTTCCTAAGA AACCTGCTGG 120
CAGAGTGCCT GCATGTCCCT CACCTTATTG GTGTCTCACA GCCACTCTGG TCACAGATGA 180
AGAAGCAACT CAAGTGGCAG CTGGACCGTG ACAGCACCAT GAGGAGCTGA GCCTTGTGGG 240
GAGAGCACTG TGTCTGGAGT CCCAGGCTGC TGTGTGACCC TGGGCAATTT GCAAAACCTT 300
TCTGAGCCTG TTTCAAATGA AAATGATGCT TCGTGGGATT GTCGTAGTCA ATGAGGGCTG 360
GGCACAGTGG CTCACACCTG TAATCTCAGC ACTTTGGGAG GCCAAGGAGG GCGGATGACT 420
TGAGGTGAGG AGTTCAAGAC CAGCCTGGCC AACATGGAGA AACCCTGTCT CTACTAAAAA 480
CAAAACAAAA CAAAACAAAA ACAAAAATTT GCCGGATGTG GTGGTGCATG CCTGTAATCT 540
CAGCTACTCG GGAGGCTGAC AGAGAATTGC TTGAACTCAG GAAGCAAAGA TTGCAGTGAG 600
CCAAGATTAC GCCAGGACAC TCCAGTCTGA GTGACAGAGT GAGACGTTGT CTCAAAAAAA 660
AAAAAAAATG GTGGCCAACG CGGTGGCTCA CACCTGTAAT CCCAGGACTT TGGGAGGCCG 720
AGGCAGGCAG ATCATTTGAG GTCAGAAGTT AGAGACCAGC CTGGCCAACA TGGTGAAACC 780
CTGTCTCTAC TAAAAATACA AAAATTAGCC TCTCATGTGG CAGGCACCTG TAGTCCCAGC 840
TGCTCAGGAG GCTGAGGCAG GAGAATCACT TGAACCCAGG AGGCAGAGTT TGCGCCACTG 900
CACTCTAGCC TGGGTGCAGA GCGAGACTCT GCCTCAAAAA AAAGAAAAAA GTCAATGAAA 960
GATATTTAAA CTGCAGGTGA TCCTGGGAAA TGACAGTGTC CTCCCCAGCC CCTTGCTCTA 1020
ATTCTTGCGC TAGGCCCTCC AAGGATGAGG GGAGGGGCCA TGCCCTCAGA AGCTTGTGGC 1080
TTCCTTGGAG AGGCAGACCA CTCCCTCATT GTGCCAGATG TCAAAGTGTG GTGCTGGAGG 1140
TCGAGGAGAG AGGGCTGGGT GACTCAGAAG CCTCACGGGA GTGAACTGGC CCTGGCCTGG 1200
CAGGCTGTGC TCCCTAGAAA CTAGAGGGGA GGAGGAGGCA GGAGGCTCAG ACAAGTCTTC 1260
TTTGAAGGAG TATAGTGGGA ATACCCCAAC AGGCCTTCAC TCACTCAAGA AACACTTGCA 1320
GGACGATGGA GTGGGAAGGG TGCCATGGAC AGGGCAATGG GTCAGACCTT GCTCTCTTGG 1380
AAGTGCCCCC ATGCAGCCAG CAGTGTCTTG GGAGCCAAGC TGAGAATGCC TGATGCTACC 1440
CTCTGTCTGT TCCATCCCTC TCCTACCCTC ACCCCCCACT CCCATTTAGG ACCCCACTGG 1500
GAGAAGGGAG GGTGGGCAGG AAGTGCTGAG CCCTGGGTTT GGAGGAGGGA CAGGGCTGGG 1560
CTGAGAGGAC CTGTTCCCAG GCCTAACCAA AACTGTTTCA TTCACCAGCA GCCCTAGGGT 1620
GAGGGGCTTG GATGGACCTT GGAGGTTGGG AGTTCATTCA TTCTAGTGGA ACAGGCAGAA 1680
ATTAATCAAA TAATCATGTG TAAATAGGGC CCATAGGAAG GACGCAAAGG CCTGTGTGTG 1740
CAGGCCAGAA AAAGGCTATC CACACAGGGT GGCCAGGACA CTTTCTCCTG TAAGGAAGGG 1800
ATGCACCAGC CAGGCCTGAA AGAATGAGTA AGAGTTGGAG GATGGAGGTG GGGCAATAAG 1860
GTAGGGAGCG AGCTGAAAAT TGCAGGCAAA GGATATAACA CATGCCCCAA GGCAGGAGGG 1920
TACAGGAGGC TGGAGTGCGT GGGAGGGAGG CAGTAGAACC AAGATGGGGG TGGAGAACAG 1980
GCCGCACTCT GCTGCACTTT GAGGACCATG GGAGAGCATT CAGTCCTTAC CCAAGAGCAA 2040
TCAAAAGCCG CTGAAGACCT TGATTTTGGA GTCAGGGTTG GGATCGGCGG GAGGGGAGGG 2100
GGGGCGGTGG CCAGGCAGTG ATGTCACAGA CACAGTCCTT CCCAGGACAC ATCTGGGAGC 2160
CCAGTAGGCT GAGAACCAGA ATGCAGTCAG CCCCCTCCCA TGGAGGAGCA CTTCTCCAGG 2220
CTGGGGAGAG CCCCTTCCCC TCCTGCCGTA CCCTGGTGGA GCCAGCCCAC TGGCCTTGTA 2280
CCAGGTGCAC TCGGTGAGTG GTTGGTGGGA GATTCTAACC CTGGGCTCAG GCCTAGCTGT 2340
TTGTGTGTGA GCTGGAGACC CACCGAGCAG CAGCAGCAGC AGCAGCAGCC GCAGCAGCCG 2400
CCACCAGATT TGCAGCCCAA GCCCCAGATT CCAGTGTCAG CCTCGCTGCA GCTGGTTTCC 2460
TGCCGTGTGC TTTTGTGAGC CGACACAAAG CAGATGGATG TGCACAGAGC CCAGCGCACA 2520
GGCCCATGGC TCCCTGCGCA CAGCCTGCTG AAGTCCTGTG ACCCCGGCAA GGGGAAGGGC 2580
TCATTAGGGA AGGTTTTCAG AGCCCTGACT AGCAGAGATG AATAGGACCT TGTGTTTGAT 2640
CCCAGAAACT GCTTCACTTG CCAGAACTAA CAGAATGGCT AAAATAACCA GCCTTGCAAG 2700
TGTGCACATG TGGTGCGGTG GCTGTGTTGG GTGGGTTGGC ATGTCACTGT GGGCCTGAGC 2760
AAGTACCCAG AAGAGCAGGA TTAGACGATG TGACCAGGTC AGGGCTGATG GAAACCTGAC 2820
CACTTCTCTC TTTTTTGACT 2840
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