Tag | Content |
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EnhancerAtlas ID | HS197-02708 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr10:64875160-64876670 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr10:64875211-64875221 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr10:64875211-64875221 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr10:64875288-64875303 | TGATCTCTTGACCTT | - | 6.93 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I063113 | chr10 | 64873341 | 64876466 |
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Enhancer Sequence | CCGGGTTCAA GCGATTCTCC TGCCTCAGCC TCCTGAGAAG CTGGGACTAC AGGCACGTGC 60 CATCACGCCC AGCTAATTTT TGTATTTTTA GTAGAGACAG GGTTTCACCA TGTTGGCCAG 120 GATGGTCTTG ATCTCTTGAC CTTGTGATCC ACCTGCCTTG GCCTCCCAAG TGCTGGGATT 180 ACAGGTGTGA GCCACAGCAC CCAGCTGAAG TTATATTTTA TAGATAGAAA AAAGGCAGCA 240 CTACTGGTGC ACCAGAAGCT GAGTGGTCCA AGGACATTAG GATTCTGGAG GGTTCGCTTC 300 AGCTTCCTTT TTTGAGAAAC ACTAACTTAG TACAAAGTCG ATTGAATCAT TGCCTTTCTG 360 CATTTATTTG ACTGCCGTTT CCCAAATGTC AGCTTACTGA ATAAAAAACT ACCCTGAAAT 420 TCTGCTTTCC TTGGACTCTC CTCTATTGAA CTTGGTTGAA TAGAATGCCT GACTCCTGCC 480 TAACTTGGCT TTGTTCACCC TGGCTCAGGC TGAAGCAACT GGACAAGTTG GCTCAGAGTC 540 CGAGGAGTTA GAGCCTGCTG ACCTCACAGC TACCCTCCCC CTTCTCACAT GGCCAGTTCC 600 TGCCCAGTCT AGTTTGTGAA TAGTTCTTGG AAAATACCCT GGAGGAGAAT AGAGTCACTA 660 ACAATAGCGA CTCTCTTTTT AGCCTGAACC TCTTAGTACT CAGGACTGTG AACCTAGGAA 720 AACCAAAAAT AACAAATGTA ATTGCAGTGG GTTACCCTCT ATTTCTATTA TTACCAACAT 780 CCAGTCATTC TGGTAGATAT TTAGCTGCTT GTCGTGGAAA AATAACTGGG TTTATAACCA 840 GACAGAGCTA GATTCAAGAC CTAGCTCAGC CATTTATTAA TTTTATGACA TTGGACAAGT 900 CCCTAATTTG AGCCCGTTAG AATTGAAAGA GGGAATGTAC ATGTAAGTGC TTGGAAACGT 960 GCAAAGTATT ATACAGTACA AAGTCAAACC ATTAATATTG GGAAATAGGG ATAATTTGAA 1020 AGTTTCAGGA AACAGAATAA TTTAATTGTT CAAAAAACAC TTGAATCAGC CCGAAGCAAA 1080 ATGGGGCTTA CTAGTCAACA CCAGTCTTAA AAATAAACAA CTAAACTATA CTGTAGTTAG 1140 TTTCTGTTTA AAGTTAAAGG CAGTCTTCCC TTTTGTTCAT GATGAAGTTG GAAATGGGGA 1200 AGGACTTATC AGATCCTTTC ATATCAGGGA ATGACGCAGA AGGATGATGG GCCCTCACAC 1260 CTATTAAGTA CAGGAAAGAT GGCCATTGCT TACATGCTGG CTCTGCTGGC AAACTGTTTT 1320 TTTTTTTTTT TTCTCTGAAG TTAAGCCCTT GTTTTTGCCA CTTAGTATTT TTATTTTATA 1380 TATAATGAAA GGGGTTGGTT CTTCAGACTT GGGCATATTT TTACCCTATA TCACTCTTGT 1440 GCATATATAA AAAGGGAAAC AGGCCAGGCA TGGTGACTCA TACCTGTAAT CCCAGCACAT 1500 TGGGAGGCCG 1510
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