Tag | Content |
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EnhancerAtlas ID | HS158-51981 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr7:55159050-55160210 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr7:55159665-55159680 | TATTAATGATTAATC | - | 6 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_24220 | chr7:55159074-55159630 | Colon_Crypt_2 | SE_28434 | chr7:55158731-55160407 | Fetal_Intestine | SE_29348 | chr7:55158656-55159965 | Fetal_Intestine_Large | SE_31784 | chr7:55158651-55160280 | Gastric | SE_42526 | chr7:55159015-55159677 | Lung | SE_45557 | chr7:55158979-55160149 | Osteoblasts | SE_47162 | chr7:55158971-55160370 | Panc1 | SE_48241 | chr7:55159048-55162407 | Psoas_Muscle | SE_51484 | chr7:55158952-55161413 | Skeletal_Muscle |
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| 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 |
GH07I055091 | chr7 | 55158997 | 55160115 |
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Enhancer Sequence | TGATAGTGGT TCCTAATGCA GTGAAAGATG TGTAAGTCAA AGATTTGTAA CCAGCCAGGG 60 AATGAGAGGC GAAGCCATAG CTGGTGGCGG GGGCCACATC TGGGTGTGGG GAGGCCACAG 120 TTGGGTTGGG GGTGGGGCCT GCAGTTATCC ACACCCCTCC CACCTCCCTT CGACAGTACA 180 GGCTTCCTGG TTACCTTCCA GAGAGTAAGG CCAGGGAGAG TTGAATAAGT TGAGAAATGT 240 CATGTCGAAG CTATTGGTGG AAAGAGTTCC ATTAATTGAC AATACAAGTC CCTACTACAT 300 TCTAAAATCT GGTCCTGACT AGTGGCAAGC CGGGCCCAGG AGTAGCACTT AAACAATGGC 360 AGGCTTGTGT TGCTGGCAGG ATACTTCAGC CTCAGAGGAG CTGTGTGCAG CTGGGGAGAC 420 TCACACTCAG AGGATTTCAA AGCAGAGGGC ATCTCGTAGA GCAACTTATC CAAACCCTGA 480 CCCACTGTAA ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACACCCTGAG 540 AGAGAGAAAG AGAGAGAGAT AACTAAAGAG AGAGAACTAA AGTTTGGCAA AATAATACAT 600 GCTCTAATGA AGGTTTATTA ATGATTAATC TACTCCTAGC ATTTCCTAGT CCACTCTATC 660 TCCTTAAAAA AAAATTCTGG TTGCAGCCCA CTAACTTGAT TGTACAGCTG CTTAATGGAT 720 AGCAGGCTGT AATTTTCAGA GAACTGTTTA ATGCGGGCTA CCTCTGTTCT TCCATGCTGC 780 TTGTGGTTCC TGCTCTGCTC AGGACAGAAT GGGGAGGAAA ACAGGCTCTG CGGCACAATA 840 TTGGCAAGTG AAATTTTGTA AACCGGCCCT CCCTTCCTTT TGCATTTGGT CTGAAAATTC 900 AATTAGATGC TGAGTCCTAC AATGTATTTG AGAAGCCCAG GAGTGCCCTA GAGGATGAGA 960 CTGGGTGGCT CCCTGTCAGG TTGAACATTT GCCTTAATTA CTTTGGCAAG ATTTGCATCA 1020 GTGGTATTAG TCCCTGCCTC ACTTGGAGGC CTGCACTTAA GTGGCCACAT TCAGGCTCCA 1080 ATTTCCTGGT GATTTCATAG TGTAGGGCAC TTGCAATCAA AACTAGGCTT AAAGCCCAAC 1140 CCTCTTACAT TTTACCCACC 1160
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