Tag | Content |
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EnhancerAtlas ID | HS024-05481 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr16:362010-364540 |
Target genes | Number: 29 | Name | Ensembl ID |
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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) |
NEUROG2 | MA0669.1 | chr16:362408-362418 | AACATATGTC | + | 6.02 | RREB1 | MA0073.1 | chr16:363691-363711 | CCCCAAATGACCCCCACAGG | + | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 364075 | 364159 | chr16 | 363398 | 363448 | chr16 | 362545 | 362698 |
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Enhancer Sequence | CGTCAGGAAC AAGTGAATCT AAAACTCACC TAACACTTGC CTCGGGGTTT GTTGAAGTGT 60 CCTGAAGCCA CCAACCTACT GGTTTCTTAG ACATGATACT TGGATTGGGT AACCTCCACA 120 GGCCTCCGTG GATTAGACAC TGACCCCACA TCTGTGTCCA CAGCCCACAG CCTCTCGAGT 180 GCCATGTGGA ATGTTGTGAG CTTGCCGCCA GCACAAAAGC TGAGGGCAGC TGCCCCACCG 240 GAATGATGCT CTTCACCTGT CCACTTTTTA CCTCTGATTT GCTTTCGAGT ACGTGTAGCA 300 ATTTCACATT CCAAATTGTT AAACACTTCA GTACAAACCA AGATGAACAG AATATCAAGA 360 AAAAAAATAC CTATTTATTT TAGGTCCTCC CTTTAGGAAA CATATGTCCC TTTTCTTGGA 420 GAGAATTAGG AGACTTTTTG AGAAAACTGA GTTGGCAGGT TACTTTTTGT TGTAGTAACA 480 GAGTTTTGGG GAAGAGGGAA ACCAGATGCT AGGATGCATG TCAGGCGCTC CGTGGGCTGC 540 ACTGCACCCA ACCACCTGGC CCGAGGCTTC AGGACCACGG CAGGCACTGC TTCAACTCCA 600 GTAACCTCAA GTCAGGTGCT GCTAAAATCA CGTCAACATT TTATTTTGAA GATTCAAAAT 660 TAAACGAGGA TGAAAGAAAC CAGGAGAAGC CACACACAGC AGCTCTGCCC GGAAGGGGCA 720 GGGAGCTGCC CCTGCACTAC CACAGCTACC TGGGGAAAAA CCAAGGGGCC AAGACCTACG 780 GCAATGTGGG CTGGCTGAAT CTGGTTCAGA AACAGAATGT GACAACTTGT TCTCCTCATC 840 TGAAATTCAG GTTTTGGAAA AATGTTTAAA GACAGGCAAA TGAAAAGAAC AAACCAGCCA 900 GGCACAGTGG CTCATGCCCA TAATCCCAGC ACTCGTGAGG CTGAAGTGGG TGCAGTTTGC 960 GCCCAGGAGT TGGAGACTGC ATAGTGAGGC CTCGTCTCCA CAAAAATAAT CATCATCATC 1020 AGCCGGATGC AGTGGCTCAT GCCCGTAATC CCAGCACTCA TGAGGCTGAA GTGGGTGCAC 1080 CGTTTGAGCC TCGGAGTTCG AGACTGCATA GTGAGGCCTC GTCTCCACAA AAATTATAAT 1140 AATCATTAGC CAGGCGTGGT GGCGCACGCT TGTAGCCTCA GCAACTCTGA AGGCTGAGGC 1200 AGAATTGCTT GGGACCAGGA GACAGAAGCT ACAGTAAGCC AAGATCGCAC CATTGCAGTC 1260 CAGCCTGGGT GACAGTGAGA TCCTGTCTCA AAATGAAAAG AACCATAAAA ATGGTACATA 1320 CAGTGGGACC ATCACTTAAA ACATATTCAT AAAAAGATGG GCAGAATCAC CAGTAGGTGA 1380 GAAGTCCCTC TCTCCTCCTC CAGCCCTATC CAGATCTCCA GGCTTTCCTC ATGGAGAACC 1440 CAGCTAAGCG GGAAAGACAT CTGGGACACC ACTGGCCGCA GTGGGGATGG AGGGTGGTGG 1500 TCCGCGGGCT CCAGCTGCTC ACAAGTTCAT AGCCGCTGGC TTCCTCCAAT GCTGAGGCTG 1560 CTGCAGGGAG ACCCTGGTTC CTGCGGCTCG GCCCCAGCCC TGGCTAGGAT GGCTGGTGGG 1620 CAGGTGGCGT GTGGCGCACA GACCAGAGCT GGGAAGGTCT GAGCTTCATG GGTAACCAAA 1680 ACCCCAAATG ACCCCCACAG GCTGGCAGCC AGTGCCCTAC TGCAACAAGA CTGTTGGCAT 1740 CATCTAATGG CTGGGGTGTA CATAGGTCCC AAAAAGCCAG CTGCGAAGCA CAGGGGAAGA 1800 GGTCATAAAA CAAGCACGTT CCTACACATG GGGTTTCCCT GGACAATGAA AGAATAAGCT 1860 TCTGCCTGTC ACCTCGAGCG TCACACATGT GTGGCCCAGG CCTCAGCACA ACCACAGCAT 1920 CTTCCCTCAC TCCTGCTCCC AGCCCCTTGC CAAGTGGGTG ACAGGGACAA GACAGGACCC 1980 TGTACTGCAC CAGCGTCGGC AGAAACGCCA CCCTCAGGGA CCACATCACT CGCCACAGCC 2040 AGTGGTGAGG CAGCTGGCCT GTGCCTGTCT TTAAGCTGAA ACCCCAGACT CTGAAAACCA 2100 AAGAGCAAAC TCTAGCCCGG GCAGCCTACA GACTGTCTTA GGTTCACCCT CGATCCTTCC 2160 TCATAGGGAG GTCCCAGCAG CCCTGGTCAC AGAGAGAAGC AACCGACACA AAGCTGAGCC 2220 CTCACTTGTA CTGCTTGGAG GACAGCCTCT GCGGTACAGC CTGCCTGCAT GTCCAGACGC 2280 ACTCTCACTG AGACCTGGGG AGCCAGGAAA CACTTTTCCT GAAGACAAAG CCCAGGCATC 2340 TCTGGGTCAG CACGAAGCCC CCTCTGAGCT GGCCGCGCTC TGCAGCAGGG TGGGACTTAC 2400 ACGCTGCCAT CCGCAAGAAA CAGGGTGTCT GGGGCAGGAC TTACACATTG CTGTCCTCAA 2460 GGGACAAGGT GTCTGGGACC GGACTTACAC ACTGCTGTCC GTGAGGGACT GGGTATCCGG 2520 GGCGGGACTT 2530
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