Tag | Content |
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EnhancerAtlas ID | HS165-00567 | Organism | Homo sapiens | Tissue/cell | Ramos | Coordinate | chr1:86127000-86128540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG1 | MA0623.2 | chr1:86128479-86128489 | GACATATGTC | + | 6.02 | NEUROG1 | MA0623.2 | chr1:86128479-86128489 | GACATATGTC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGTTTCCAT GCTTGAAAAT GGGGATAATG ACAGTATCAC TTCAGAGAGT TACTGTGAGG 60 GCTAAATGAT AAAACACAGA AACTGCTCAC TCATTTATTT AAGCCCTAAG CACATGTGTT 120 TGTTTTATAT TTTTATTTAC CAAAAATAAC AACACTTTCC TATAGAAACT CTAGTTCAGG 180 ACAAAGTCAC TGGATTTCAT TAGCAGTGAA CATACTGCCT TTATGTGCAT TTTGCATTTT 240 AAATGTAGCC TTACAACTTT CTGTATGACC TTCAAATCAT TATTTTATTG TCACATTTAC 300 TTCCAAGAAG ATAAAGGTAC TTTGAATGTT TCTGTTTCCA CTATCTTGAA GCAAGTTTTA 360 AGAGCCCAGC TTTGCACTGC CTAAAACACT TAGGTTTAGC TCCTTTGCAA GCCATTAAGC 420 TACTGAATCC TAAGGGACAG CTTTATCTTT TTGAAATTTT CACAAACTCT GGTATTTCCA 480 TTAATATAAT GTCTCTGCTA CCATAAGACA AACTACTTAG GTTTGGAGGA ATTAAGATAC 540 TAACATTTGT CTTTTCTCTT GCCCTCTGGG ACCCTTCTTA GACATTTCCT CTTGTTATTT 600 CACTTGCTCA CCCTCACAGG TTCACTGGCT GACCCTGCTC TGGGCAGCCT CATGGGCGCA 660 TTATGAGGGC AGAACGGCTC AGTGGGCCAA ACAGGTGTTA CAGTGACATA TATAAATAAA 720 AGTTGTCATG ATAATCAAGG GTGTGCTTTT AATCTTGACT CTGTCACTAA CTTTCAAAGA 780 AACAGGCCAA GCTCTTGAAC TTCTTTCTCT GTACTTTATT AGCAAATTAG TGTGCTTTAA 840 AAAAAAAAAA AAAACCTCCT CATAACCACA AAAGACAAGT TTTTAAAGAA ACGAAATCAC 900 AAACCACTTT ATGTCCCATC TGATCACTGA CACTCCATGG ATCATCGCCC CTTCCACCTG 960 CTAAAAAATA CCAAAACTAA GTTTGAATTT CTCCAAATTT AGCAATCTAG TAGCAGGCCC 1020 TAGGCCACAG TATTTTTCCA CTAAAATAAG ATCATTGAAT TAGGTGATCA CTAAGATCCC 1080 TTCAGCTCTA AATTTCTACA ATTTTTGATA CTTAACTATA TTTTTTCACA GTTGTATTTA 1140 TTTCTCAATC TAGGTTTCTA GATTAAAAGT TCAACTAAAT TATTCCAAAA AAGTTTTAAT 1200 TCTTCTTTTA TTTAAACTTT AAAAGGTATT ATTTAAAATT TCTCCAAATA ATACTTCTGT 1260 GTAACAATTT TTGCAACTCC TAATGTTCAA GTCATATAGA AAAGGATTTT GCCATAGTTA 1320 ATCTTTTTCT CACCCAATCT CTCTTAGTTT TCATATTTTA AAAATCACAG TAGTTAAGTT 1380 AGTGGTTTGA TGCACTTTGT TTTGGGATTT TTATATATCC ACATAAATGA GGACGATACC 1440 TGCTTGACAT GGAGAGTAGA TCATGAATTG TGTAGTACAG ACATATGTCT TAATTCAGAA 1500 AGCTCACCAG TTCAGAACTG CATTTGGTAA ATTATCCTAT 1540
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