Tag | Content |
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EnhancerAtlas ID | HS176-37967 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:98759710-98760790 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:98759885-98759900 | TGAACTCCTGACCTC | - | 6.22 | TBX21 | MA0690.1 | chr7:98760066-98760076 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr7:98760065-98760076 | ATTCACACCTT | - | 6.02 |
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| 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 |
GH07I099162 | chr7 | 98759810 | 98760910 |
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Enhancer Sequence | CAGGCTGGAG TGCAGTGGTG CAATCTCAGC TCACTACAAC CTCCACCTCC TGGGTTCAAG 60 TGATTCTCCA ACCTTGCCTC CCGAGTAACT GGGATTACAG GCATGTGCCA CCATACCCAG 120 CTAATTTTGT ATTTTTAGCA GAGACAGGGT CTCACTATGT TGGCCAGGCT GGTCTTGAAC 180 TCCTGACCTC AGGTGATCTA CCTGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCATGA 240 GCCACCATGC CCAGCTGAGA ATTGCATTCT TTGAGGTACA TTACAATTTC TGGGCAAATG 300 CAAAAGGTCA AAGTTGTTCC AGTTCAGTGT TCACACCGTA AACCAACCTA TAGCCATTCA 360 CACCTTCCTT CCTCTTTGTT GCCTCACCAG TCGTCCCAAC TCCCCGAGTC TAAGCAGGTG 420 GGCACCCAGC CAGAAGGTGA CTAACACCAT CTCTTTGCAC CCAGACCATA TACCAAAGGC 480 AAATTGCTCC TTTTTTTAAA CCTTGCTAGG CAAGTCAGTA TTAGTATCTT CAAACTACAA 540 AGGCTGCTTT GTCATGCAAA GAGAAGGAAA AAAAGAGGTT GACAGTATTT TGAGCCAACA 600 AGGTTAGATC ACTCGGACAA CAGTGACTAA GCTCAACAGG GCTTCCAGCT CTTTTAATTA 660 AAAAAATTTT TTCTCAAAGA CCTATCTTTG TAAACCATCT CACCTTTCCA CCTCCCTTCA 720 ACTACAATCT ACGAATAGGG GGAAAAATGC TTTAAGATGT TGAAAAAGAA TCTGTATTCC 780 AATCAGATTC TTTGAAAAAA AGTATATGTA AGGCTGGACA CGGTAGCTCA CGCCTGTAAT 840 CCCAACACTT TGGGAGGCTG ACACAGGCAG ATCAACTGAG GTCGGGAGTT CAAGACCAGC 900 CTGATCAACA TGGAGAAACC CTAGCTCTAC TAAAAATACA AAAATTAGCT GGATGTGGTG 960 GCACACTCCT ATAATCCCAG CTACTCGGGA AGCTGAGGCA GGAGGATCAC TTGAACCTGG 1020 GAGGCGGAGG TTGCAGTGAG CCGAGACTGC GTGACTGCAC TCCAGCCTGG GCAGCAAGAG 1080
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