| Tag | Content |
|---|
EnhancerAtlas ID | HS158-00739 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:17894950-17897970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr1:17897554-17897569 | GAGTTCAAGGGCAGG | + | 6.1 | | REST | MA0138.2 | chr1:17896519-17896540 | GGAGCTGTCCTGGGTGCAGGC | - | 7.07 | | ZNF263 | MA0528.1 | chr1:17897690-17897711 | GAAGGAGGAGCGGAGGAAGGG | + | 7.14 | | ZNF263 | MA0528.1 | chr1:17897693-17897714 | GGAGGAGCGGAGGAAGGGGAG | + | 7.15 | | ZNF263 | MA0528.1 | chr1:17897686-17897707 | GGAGGAAGGAGGAGCGGAGGA | + | 7.28 | | ZNF263 | MA0528.1 | chr1:17895374-17895395 | CCTCCCTGCTCTCCCTCCCCC | - | 7.68 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00612 | chr1:17885040-17898127 | Adipose_Nuclei | | SE_01537 | chr1:17887238-17903710 | Aorta | | SE_03096 | chr1:17894836-17897293 | Bladder | | SE_06186 | chr1:17884729-17903611 | Brain_Hippocampus_Middle | | SE_23081 | chr1:17894994-17898004 | Colon_Crypt_1 | | SE_23747 | chr1:17895586-17898000 | Colon_Crypt_2 | | SE_24767 | chr1:17895440-17896896 | Colon_Crypt_3 | | SE_24767 | chr1:17897349-17897980 | Colon_Crypt_3 | | SE_26139 | chr1:17893912-17897509 | Duodenum_Smooth_Muscle | | SE_26573 | chr1:17889896-17898099 | Esophagus | | SE_28131 | chr1:17895406-17896604 | Fetal_Intestine | | SE_29073 | chr1:17895366-17896616 | Fetal_Intestine_Large | | SE_31687 | chr1:17894075-17897582 | Gastric | | SE_34117 | chr1:17894944-17897531 | HCC1954 | | SE_40808 | chr1:17894012-17898190 | Left_Ventricle | | SE_43031 | chr1:17890076-17897872 | Lung | | SE_46963 | chr1:17894194-17897822 | Ovary | | SE_47562 | chr1:17895380-17897212 | Pancreas | | SE_50079 | chr1:17894046-17898025 | Sigmoid_Colon | | SE_52601 | chr1:17894207-17897494 | Small_Intestine | | SE_54767 | chr1:17885171-17898261 | Stomach_Smooth_Muscle | | SE_57000 | chr1:17894996-17897983 | VACO_400 | | SE_57435 | chr1:17895275-17896682 | VACO_503 | | SE_65277 | chr1:17894892-17897819 | Pancreatic_islets | | SE_68684 | chr1:17894864-17898084 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I017567 | chr1 | 17893806 | 17897918 |
|
Enhancer Sequence | GGCATGATGG TGACATGGCA AAAAGGGGAA CCTGGGGGGC ACACTGGCAG GACCAGAGAT 60
TGCTTCAGAG CAGAAATGAC CTGGAGTAGA GTGGTCCCAT TTTTCACTGG GCAAGCAGTG 120
GTGTCTCTGC CTGCAGGATG TCGGGGGGTG CTTGAAGCTC ATTACACCCA GTGTGGCTTC 180
CATGCCAAGG CAGAAGGAAT ACTAGGGGGA GTTTAGGACC AGGCTGTGGG CGGCATCCGC 240
ATTGTCTGGT TCCTCGTAAG TCGCACCACA GGGTTGGTCA GCAGCAGTTC AGCTCTTGTT 300
AAAGCTGATA GGGAAAGAGG ACGGGTGTTT GGGAACAGTT CTCTTGGGGG ATCCTGGTCC 360
CGGATTTGAC TTCAACTCAG GACAACAGGA CTCAGGGCAA ATCCTTTTAA TGATTGAAGC 420
CATCCCTCCC TGCTCTCCCT CCCCCAACAC CTCCAGCCCA GTCTTCCCTG TCCCCTTCCC 480
ACAGCCCCAG TCCGCATCTT CTCAGATTGT GAAGTTAATT GCAAGGGAGT GGGATGGACC 540
CATTGGCCTG ATCCTGATGG ATCTTTCCAG TCACAGCTGA AAGACCTTGG GTCTAATCAT 600
GGATCCACCT TTGATCAGAT TCTTGGCTTT GAACAAATCT CTCTCCCTCT CTGAGCCTCA 660
GTTTCCTCCT CTGTAAAACA GGGTCAGGTA CCTGCCATTC GTGGGTTGGC TCTGCCCCTG 720
GAGGAACTGG TGGGAGGATT AGGGGAGGCA CCAGGCATCC CCTGGCCTGG AGCAGTGCTC 780
AGAGCCAACT CCCGCCAGAG GTGCCCCAGA ACAGCTGGAA CTGCACTCAC ACCCTTATCT 840
GGGGAGGACA GCACATCACT GAGGGGTGTG GTTTGAATCA TAAGTGCTGG CTGCTCTGAA 900
TTCAGCCAGA GCTATCCTGG GCTGTGTGGC TGAGGGCCCC CGGGGGTCCT GGGGCTCCAT 960
GCTGGGCTTG CATTTCAGGA GACCTCAGAT GCTGCTGGCC TGCTTGCCCT GCCGTTGTTG 1020
GGTGGGTTGA GCTGTTTTTA GCTCTAAGCT TTGCAAAGGC TGTTTCTTTC CTGCCCAGAG 1080
CTCCCTCGTG GGACAGAGTG AACAGGCCCC TCCCTGCCAG ACAGAGATTG GGCCTGAAGA 1140
AAGAGCTTGG AGCCAGATGG GACCCTGTGG GCTTTGAAAG GGAGGCCTGG TTTGCTCTCT 1200
GTGGCCTGCC AACCTGGGAC ACCGGTGCCC AGCCTTGCTC CTTCCCTGGG AAACTGAATA 1260
GACGCCAGGG TCTCACACCT GCCCCGTGGG AAAGGCTGGG GTATGTGCCT GCCTGGTGAC 1320
GGTGGCAGCC GCGGAGGCTC GCGGATCCTG TCCCCTTTGC CGGCCACATG CTTCTGACTC 1380
ATCAGAGGAA GAATGTGGTC TTTTTGGGAG AGAGTTTTTA AAAATAGTCC AAGTCCTCCT 1440
CTGGCCCTGT CCCACTCCTC CCCTTCTGAC CATTTCCTGG CATCAGCCCC AGACCTCTTT 1500
CCACTCTGGT TTTGGGGAAC TGCCCCTTTG CAACTTGGCT GTGAATCTGT TTGTGAACCT 1560
TACTGGGGAG GAGCTGTCCT GGGTGCAGGC TGGTTTCAGA AGGGAGGGGC CCAGCTGTGG 1620
CCGCCTCCTC CCCAGGGGCC CGACTTGGGA CGAGGGATTT CTGCATTCCT TTGGCAACTG 1680
TGCCTTGGGT CGCCTGTGTG TCAGGCCTGT GCCATGGGTG CAGATAAGAG CGGTGAACAG 1740
TGGTCACAGT CCTGCCTTCA TGGAGTCCAC ATTCTCATAG GAGGAAACTG ATAAATAACT 1800
AAAATTTGTA GTTGCCAGAG GTGTTAAATC CTGTGAGGAT GGGGACACTG GGTCAGGGCA 1860
TGTGTGTGGG CTGTCAGGAG AAGGCCTCTG ATACAGCGAC CTTGGAGCAG AGCCCTGAAG 1920
GTGAGGGCAG CAGTGTGTGG GTATCTGGGG GAACAGCATT TCAGGCAGTG GGAACAGCAA 1980
GTGCAAAGGC CCTGAGGCAG AAACATGCTT GGGGCATTCA GGGAGCTGGA AGGTGGTGGT 2040
GACTAGAGTG AGCTGTGTGG AGAGAGGTAG GACATGAAGT CGGGGGGGTT GTGGGGGCTC 2100
TGACACGTGG GGCCTCAGAG ATCAAGATGA GGGCTTGGGT CTTCCTTAAA TGAGGTGAGA 2160
AAACATTCCA GGCTCTGAGC GGAGGATGAA CTTGGCCGCT GTGCTGAGAA CAACATGTCA 2220
GGGCAGGGGT AGAGGTGAGA GCAGAGGGAC TGGTCAGGAG GCGTTTTGAA TAGCCCAGGT 2280
GAGAGATGAT GGTGGTTTGG GCCATGGTGG TACTGTGGAG GGGGTGAGAT GCGCTCGGAT 2340
TCTGGGCGTA TGTTGAAGGT AGAGCCAGCA GGTTTGCTGA AGGGTGGGCC CTGGGTGTGA 2400
GACAGAGGTG TCAAGGATGA CTCCAAGGTT TTGGCCTTAG CAGCTGGTGG GATGGTGCTA 2460
GCAAGCGGGA TGGGAAGACT GGGAGGAGCA GGGTTCTTTG TTCTGGCAGC ATGGTGATCA 2520
GGAGGTGGGT ATGGGCACGT TAAGGCTGAG ATGCCCGATC AATCACTGAG TGAAGACACA 2580
GAGCAGGCAG AGGGGCAGAG CCTGGAGTTC AAGGGCAGGA CAGGCTGGAG GCATCACTAT 2640
GGCCATGGCT TAGGACCCAC GAAGTGAGCC AGGTGACCCA GGTGGCCCAG GGAGGAGCCG 2700
CGGTGTAGCC TGAACCTGGG AACTGCCAAC CTGGAGGGAG GAAGGAGGAG CGGAGGAAGG 2760
GGAGCTGGAG CGAGACGTGA AAGAAGGGAG CAGCTGGCAG GTCAGGCAGA ATGGGGACCG 2820
AGATGCTCCT CTCTCCCCAT CCTGGTCCAT CAGAACCGGT GTAGTGGAGG CCGCAGGTGA 2880
CCTCGTGAGC TGGCTGGCAA AGCGGTGGGC ACACACTTGG TTGGGAATAG GTAGCTCAGC 2940
ACAGAATAGG AGACAGGGAC AGGAGACGGA GCATGGGCAC TCCTCGGGGA AGTCTTGTAA 3000
AGGGGAGCAG AGAAATGGGG 3020
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