Tag | Content |
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EnhancerAtlas ID | HS175-02280 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr1:180393940-180395420 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG1 | MA0623.2 | chr1:180394517-180394527 | GACATATGTC | + | 6.02 | NEUROG1 | MA0623.2 | chr1:180394517-180394527 | GACATATGTC | - | 6.02 | PBX1 | MA0070.1 | chr1:180395268-180395280 | CCATCAATCATT | + | 6.07 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGTTGATGA ATGACCCTTG GTTCAGAAAG GGCTAGATTT GTGTACATGC TTGGTTGGCA 60 TCATGACACT GAGCACACAG GAGGTAAATG AAGCACGCTA GAAAAGGGTG AATATGAGAG 120 CCAGGAGACT CTTACAACAG TTACTGTTTA TGTCAAGACC CACATGTCCC AGGGGACCCA 180 TTTTCACATA ATCTATAATT ATCTCTTCGC TTTAATCGCC TTGTCATTCC TGAGGTTCTC 240 ATGGGCACTG GAAGAGGAAA AGCTCATTAA CTAAACCTTT TCTCCTCTCT CCAGCCACCC 300 ATGGCTTTTA ATTGCTTGGT GTGTTATTAT CTAGGAGTGC AACTGGAATC ATTTTCATAA 360 GAAAGGGAGG TAGAGAGGAG GAAGGGAGCC ATGAGTCCCT GAGGTATGCA CCAAAGACAA 420 ACCTTTGCTT TCTCAATTAT TTATGCCAGC TGAGGTTTTA CAGGCTGAAT AAATCCATAA 480 CTCAAGTTCA TTCTGAGCAG TCAGATTCTC CAGGGGGAGT TGCCCACTTG CCTATACCCA 540 CTTGTGTAGT CCTCAAAGAA TAACCAGAAT TTAACAAGAC ATATGTCATC CAATTTATCA 600 CCTATCACCA AGGTGTTAAC ACAATGTTGA TCATAGGCAA CATGGTGAAA TAGAGAAGTA 660 TTACACTACC ACCAGCCAAA CAGATGGAGG GAAGCTTTTT GGTGCTAAAG GCAGTGGTAT 720 CATTAGGATA GTGGTGTTCC AGAATGACGG CCTGTTAAAT GCATAAAAAT CCAAATATTC 780 ATTTTTTAAA ACACAAATAT GTAGAACACA TACTCTTGAA GCTTAAGAAT CTTTAAGTAG 840 ATTTGTTAAA AACAGGCTGC AATGTAACAA TGTGAAGCTT TGAATGAATA AATAGAATTT 900 TATAACATCT GATTTTAGAA GTAATTTACA ATAAAACTAT ACACGTTACA GCTTTTTCTC 960 CAATCATATC TCTTTCAGGA AAATTTTAGA GTATAATTTA TGCATGACAG GCTTTTATGC 1020 TACTTCCAAG TTAGTTCATA TTTCACCAAG AATACAAAAT TAAAGCATAA AACAATCACT 1080 TTCATTCTAA TTTTTTATAC TTATATTCTT CCATTTATAA TCAGGACTAG ACAGCAGCCA 1140 ATGAAAAGAT ATTTGGGAAA TATTTTCAAA ATCCATTATT GTTTAAAAAT GGAAACTTTA 1200 TAAGTCAATG ATTAAAGCAT CTCTTTGAAA TTCTACAGGC TTTTGTGTCT GACCACAAGC 1260 AGCAACCTCT TGTATTTTCT GCCAAAACAC TTCATTTGTC TCACAGAACA ACTAATCAAT 1320 TCCAGAGCCC ATCAATCATT TCAGTTGTAT ACTAGGACTG GTCTTGCTTA GAGAAGGTCC 1380 AGATGGCTGT CTGTGTAAGC AGAATTAATA AAATTCTAAT AGATTACATG ACATCAAACT 1440 ACAAAATATA ACAGGGAGGA TCAAATCTTA TTGCAGGGTG 1480
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