| Tag | Content |
|---|
EnhancerAtlas ID | HS176-02371 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr1:150294040-150295470 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr1:150294215-150294226 | GGGCGGGAAGG | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTGAGTAGT GGCCCCGGGC CCACAGAGGG TAATTCCAGT CCGCGCCACT GTGGCCGGGG 60
ACTCAGTCCA AGGGGAGGAC CGAAGCGGGA GGGTTCAGCG GGAAGGAGTG TGAAAGGAGT 120
ACCTGGTTTG GTGGGAGAAG AGGTTGGAAT GAGATTGTTG AGAGGAAAAG GGCGGGGGCG 180
GGAAGGAGAC CGGGTTGGGA GACCAGCTCT GGGGTGAGGA GTTTAGGTAG AACAAGGTAG 240
AGTAAGAGAC TGGTTGGAGT GACGGAGAGA GTAAAAATGA AGATTAGCGG GGGAGTGGGG 300
GGCTGCAGAG GGAAACTCAG GTTGTAGCAA ACAAGAGCAC GGAGTAAGGA ATTCCTTCTG 360
AAGACTGGAT TTGGATTCTG CTGCCTGCTC ATTGAGAGGA GAGATCATTG TACCTCGCTT 420
TCCTTCCGCA CCCCCACTAC CCCCGCACCT CGCAGTTATT GTTGAGCATT TGATTAGTGA 480
CAAGGCTAAT TACCGTTTGA AACTTTTTTA TCCATTGGCT GTTTAGTTTG CACGTCATCT 540
TATGGAGGTA ACAGTGGCAC CTCATTTATT GCTTTGGGCT TTCAAATTGC TTATACTTTC 600
TAGCCTATCA TTCAATTCTA GTGGAATATA AGACCCGTTA AGGTGAGGAC TCTTGTTAGT 660
TTTGCTCACT GTTTTATGTA TCCACCGCAC CTAGTACATT GCTTGACACT TAGTAGTTAC 720
TCAATAAATA TTTATTGAAT GAATTAGGAT GTAAATATGG CAGTACTCAT TTTGTAAGAT 780
GGTAAACTGT GGCTCCAAAG AATTACTTAA CTTGCCCAAG GGCTTGTAAA TGGTGGGGCT 840
CAGTGTCCCA ACTGTTTCTG TGTGAACTCT TGTTTTCACT TTCTATGGCA TCTGGATATG 900
CCGCTTTTGT GCAATACATG TGTAATATGT AGAAATTGGT ACGCTGTATG TCTACTCATT 960
GTGGGGTAAT AGAACCACCA TAGAATTACT CACGTAACTT GTCACTGAGG CAGAAAATCT 1020
TTCAGTCTTA GTTTCATCAC TTCAATCTAC TAGCTTCCTT TGGATATACC AAAAGTGAGT 1080
CTATTTGGCA GCAAGTCTTA TAGACTCTAG TATAGAGGCT AAACTTACCA AGAATGTAGA 1140
AGTTAATCAG ACTGGATTTT TTGGAGAAAA GATGTCTTAA AACATCTTGA AAGATGATTC 1200
CCAGATCTTT GATAAGTGGC ACTGCTGGGA ATAGCTGAGC TTGGAAATTG AGGTCAGTCA 1260
ATTTATTGAC TCCCATTTAG ACACCTTTTT TTTTTTTTCC CCGGGACGGA GTCTTGCTCT 1320
GTCGCCCAGG CTGGAGTGCA GTGGTGCGAT CTCGGCTCAC TGCAACCTCC GCCTTCCATG 1380
TTCAAGGGAT TCTCCTGTCT CAGCCTCCAG AGTAGCTGGG ATTACAGGTG 1430
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