| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02835 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr1:170591440-170592900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:170592067-170592088 | TTTCCCTCCATTCCATCCTCC | - | 6.4 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I170622 | chr1 | 170591588 | 170592946 |
| Enhancer Sequence | TTTTGCCCAT TTTTCCCACT GGATTGTTTG ACTTTGTGAA ATTAATTTCT AGCAGTTTAT 60
AATATATTCT AAATGTCATT TCTTTGACAA TTATATGCCT TGCAAATAAC TTCTCTCTAC 120
TATGTCTCTT TAATGATTTA TAGACTGCTG TATATAATGG CACATCTCAC CTCAATTCCT 180
TAAATCAGCC TCATCCACTA TACATAGTTG ATGCCAAAAA GGAAATATTA CAGCAACTTC 240
ACTGTGCTTT TCTATCAACC TCATTCTTGT TCAACTTCAG TTATACCTTG CTTCTAGCCC 300
TTGGCTCTGT TTTTCTTTGG CCTCAAATCC AATCTTTTGT ATGACATTTG AACTTGCATA 360
TCCAAGTTTT TATATTCTGT GCTTCCTGAA AATGTTGTTC AGCACTCAAC CTTTGTCATC 420
TCATCTTTTT CCTTCTTGTG TAGATTCTCT GGATCTTATA TAATTTATAT CCCATGCTTT 480
CATGATTGTG ATAAGCTAGA TCCTTTGGTC TAGCATTGAA ATTTCTCTTA AATGCTAAAT 540
CTTTAATAAA TGAATTTGTT TTCTTCAGAC ATATATTTCT ATCATAGATC ATCTTATTAA 600
TGTATTTTAT GACTTCTTTA TTATCTGTTT CCCTCCATTC CATCCTCCTA CAAGAATGTA 660
AACTTTATGA GAGCAAGAAC TTTGTCTTTT CACCACAGTA TTTTCAATAA TTTTTGAATG 720
CAAAAATGAA TCCAGATAAT GTTCTTTGCA TGATTTCTTA TTTTTGGAAA CCCAGCACAA 780
GTCTTTCTAA CTAAGGTTCT ATACCGTTCT CACATCATAA TATGTAGCTA GTCAATCTTC 840
ATTAATTATT TTTGTTGTAA TTTCGTTATC AGAGCACCTT TGATAAGTAT GGCAGTTTTA 900
AAACATGACT GTAAATTATT TGTCATTTCT CCCATAAAGA GGTCCGATTT GTGTACTCAT 960
TCTTGATTTG GGTGAGTTTG TGGTGCCACA GGATTTTTGA GACTGAGTCA TAAAAAGTCA 1020
TGCAATTTGC ACCGTGTTTG CTGGAACACT TGCTCATGGA ATCCTGAGTC ATGATGTGAT 1080
AAGTCCAACA GCATATCCTG AGGCCACCAT ACTGTGAGGA AACCCAAGCC ATATGGAGAG 1140
GTCACATGGC AACATGCAGA TCACATAGTC ACATGTAGGA GTTCTAGGTG ACAGTCCCTG 1200
CTTAGCCCAG GCTCTGATTT ATTCCTGACC AGTTCCCAGA CATGGAAGAA GCCTCTAAAT 1260
GATTCTGTCT CTCAATTGTT CAAGTCACTC CCAGTCATTT AAGTCTCTTT AGCTGAGTCC 1320
ACATATACTA TGAAGCAAAG ACAGAACATG TCCACTGTGC TCTGCCTGAA TGCTAAATGC 1380
TACCCTATAC AAAAAGGATG CCAAATTAAT TTTGAGGCCA AAATTCTATT ATGGTAGAGT 1440
GAAAAGACCA GATAAACCAC 1460
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