Tag | Content |
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EnhancerAtlas ID | HS007-07491 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:79049400-79050780 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr17:79050506-79050517 | TGGGTGTGGCT | - | 6.14 | NR2F1 | MA0017.2 | chr17:79050197-79050210 | AAAAGGTCAAGGG | + | 6.39 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_31420 | chr17:79048326-79049803 | Gastric | SE_65309 | chr17:79049313-79050100 | Pancreatic_islets | SE_69007 | chr17:79048107-79049806 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 79049912 | 79050173 | chr17 | 79050238 | 79050588 | chr17 | 79050659 | 79050768 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I081073 | chr17 | 79047747 | 79050100 |
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Enhancer Sequence | CCTTTGAGAG CGTCCTGAGT GACCCTCTCC AAGGACCCTA CCTCCACCTG TCCACCAGCC 60 CTCCTTGCCT TTAACCCTTT CAGTGCTACG CGTATCACCA CACTCCCTCT GTGCCCTTCT 120 CCCCCAGGTA GGGGCCACTT AGAACACTAT GGCAGCCTTT GGTGGGCCTC AAGTCCTGCT 180 CCTCCCCTCC GTGGGCACAT TGGGGCCCCC AGTACTGCCC AGCCTTTGCA CTGGCCAGCC 240 ACAGGCTCCA TATGAGGCCA GCTGGGCACT GCCATCTCTG TCCTGGCACG GAGGTTCTGC 300 CAGGGTCTGT GTATACTTTT TTGGGTCTGC TGGGAATTTT TTTTTTTTTT TTGTAGTGGT 360 GATGAATAAA ATGCATAACG CAGAGAAGCA GAAGTGCCTG CACCCGGGTG TTCCCTCTTG 420 CTAGTAATCC TGAGGTTTGG TAGAAGCCAG CTCCTGCTGG GGTCAGGGGC AGTGAGGCAG 480 GGGCTCCCCA GAGTACAGCC TGAGAGGCCT GGCTGCTTGG CTGGGGGGAG TGCCGAGTCT 540 CAGGTCCTGC CGGGAGGCAC AGTCCTTCCA GAATCAATCC CTGTTACCAT CTGCAGCTTA 600 ACTCATTTTA AGCTTAACCA TCTGCAGCTT AACTCATTCT TGCTTTATCT TCCCTGTGGA 660 CCAGGTCTAG CCTGGGGCAG ACAGGAGATG GCAGATGGAC ACCTGGGAGG GGCTCACTGA 720 GCTCCGCCTC TCCATCAACG GAGGCCCCGT CTAGGTTGTG GAGGATGCTT GAGAGAGCCC 780 TGATGTTCTG ACCTCCCAAA AGGTCAAGGG TGCTGGCAGC CGGTGAGACG CCGCAGTTTG 840 CTCTGCTCCC CGGGGCTGTG CTTGCCAGGA GACATTTCGG CTATAAGCAG GCGAGAATAC 900 CTCCAGAACA CACATCAGGA AGACAGATGG TGTGCAGGTG GGGCTCAGGG CTGTCATCCC 960 CTGAAGCTGC TTCTGAAAGA GCTGTTCTTG CAGCAGCACT GTTACAAAAG GCCACATGGG 1020 AAACAGCCCG CACCTCTCAG TGGATGCCGG CAGAAACGCC TCGTGTATCC ATAGGGTGAA 1080 GTTGTATTCA ACCACAAAGG ACAGGCTGGG TGTGGCTCAT ACCTGTAATC CCAGCACTTT 1140 GGGAGTCCAC TTGATCCCAG GAGTTCAAGA CCAGCCTGGG CAACATAGTG AGACCCCATG 1200 TCTACAAAAG TATCTTAAAA ATGATCTGGG CATGGTGGCA CACCCCTGTA GTCCCAGCTC 1260 CTCGAGAGGC TGGGGCCGGA GGATCCCTCG AACCCAGGAG TTGGAGGCAG CAGTGAGCCA 1320 TGATTGTGGC ACTTCACTCC AGCCTGGTGA CAGAGTGAGA CCCCTGGCTC TAAAAAGACA 1380
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