Tag | Content |
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EnhancerAtlas ID | HS176-13047 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr14:92449270-92450760 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr14:92449646-92449657 | AATAAACAATG | - | 6.02 | NFAT5 | MA0606.1 | chr14:92450390-92450400 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr14:92450390-92450400 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr14:92450390-92450400 | ATTTTCCATT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATGTGCACA CATACCCACC ACCCTTGGTC ATTACTAGTC AACTGTATCT TCAGCCAGTT 60 TCCAGATTAT GACACACAGT TTCACAGGAA TTCCTCCCTC TGTCTAGAAC ACTTTTCCCC 120 AACTTTCTGC CTTCTTAGCT ATACCTATTC ACCATTCAAG TAATTTCAAG TGAGCCCTTC 180 ACTAACCTTG TCTACCCTTC CATGCTACCA ACACCAAGTA CAAAGGATAG CTCTTTCCTT 240 TCTAAACCAT TTGTTTCATG TATTTGATGC ATGTCATCTT CCCTTCCTGC CTGACTGTAA 300 ACCTCCTGAA GGCAGGACCC TTGTCTCCTG TCTTTATTTA TATCTTTAGT TCTACTGCAG 360 TGCTTAGCAC ACAGCAAATA AACAATGAAT ATTTGAGAAG TAAGTCAAAT AATGATTGAT 420 TTTCTCTGGG AAAAGAGAAT ATCTGCAAAG AACAGAACAC TGGACAAAAA GAACAATTTA 480 TGTTCTGAAT TATGAACTCA TCCATACATA AAGAAATAAG GGCAAGGACA CAAAACACAT 540 TAACTCAAAA CATTCTTATT GCTATATCAT TTACTTTTCC CTTTAAACTT AGAGGAATTT 600 TTTTAAACTG CAATTTCTAA AATACAGTTC AGTTGAAAAA GGTTTAATTA TTTACCTAAT 660 TGACATACAC TTTTTTCTTA ACTCATATTT TGGCATTGTC TAGTATACCC AGATGTTTAT 720 ATCATCAAAA TAATTTTTTA ACCATTTATG GCAACTCAGA AAACTGCATC TGGTACTTCT 780 TATATGTTTC CTCTAAAATC ACCACTTCTG CCAAAAACAT CTATAAAGAA ATCTCTCAAA 840 AGGTTTGGGT AACAAAGCGT CTGGGAATGT ATTTGGCCTG TGTTCAACAG GACATTATAT 900 GTTTTCTTGT ATAAATCATG TCCTGGAAAA CGGAATGTCT TTATTTAAAA TAAAAACTTT 960 ACCATCCAGC ACCGTAAAGG TAGTTCCACG AAAAATATTT TAAGCTTCTT TTATATCTGT 1020 AGCTTTAAAA CATGTTTTTA TGCTTCATAT TACAGTAAGT TTTACTGGGA CTCATTTTAT 1080 ACATTCTTCT AGATTTTCTT TTAAAAAATG GTCCAAGGAA ATTTTCCATT CTCAACTCTT 1140 AGGAGACTTT TAAAAGTAGT CATTCAACCT TCTTAAAAAA AAAATCAGTT ATGCTGCCCT 1200 TTCAGATACA GGTATAAACT AGCAGACAGA CCAAAAGATC TTCCTGATGT TAGAACTAAA 1260 TTTGTATTGC TTATGAAAAC TCACTTTTCT TTGCACACCA TAAAATTCAC CACCTTTCTG 1320 AATCATAGTT ATCAAAATAA CAATATCTTG TGCTTTTTAT TTCAATTTAT CCAATCATTT 1380 TTTTTCTTTT CTTTTTTTTT TTTTTTTGGG ACCAAGTTTC ACTCTGTTGC CCAGGCTGGA 1440 GTGCAGTGGC GTGATCTCAA CTCACCGCAA CCTCCACCTC CCAGGTTCAG 1490
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