Tag | Content |
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EnhancerAtlas ID | HS184-27630 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr7:27386210-27387250 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr7:27386840-27386851 | AACCAATCAGA | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 27386657 | 27387000 | chr7 | 27386310 | 27387250 |
| | Number: 1 | ID | Chromosome | Start | End |
GH07I027346 | chr7 | 27386124 | 27387887 |
| Enhancer Sequence | AAAAAAGCCC CCCCAAACCC AGCAGGACCT CAATGATGGA AGCAAATCTG GAAAATAAGG 60 AAATCTGATA AAACATAAGC CCACCATTTT TGCCTTGTGG TGTGGGTGTT GTCCTTACCT 120 GCTGGAAAAC ACTGGCAAGT CTGTTCAGTG AGAGGCAGCC GAAGAAGGCT AGCAAATAGA 180 TTTATTAATC ATTTCAGGAA AAATGAAGAA TGCCTTTAAA GACAACACCC TCTTCTTGGC 240 TTCACAGAAT CTTTTTAGGT TTTACTGTTA ATAAGATTAA ACAGGAGATG AGCAGTAAAG 300 ATATTGAAGC AGAGTTTTTT TTATAAGAAA AAGTACACAT TAAGAATCGG GCTCCCCCAC 360 CACTTAGCTC AGCACTGTGT CCACATTCTT CTATTCAGAT TTTTTTATTG CTGTTTGCTT 420 AGGGGAAAAA GTCCCTGTTG AAAGAATGCG GGCCGGAGTA CATTAGTCAC CTTTCCAGTG 480 CTGTTTCTGT GGGACGGGGC CACGTATCCC TCCCAACTCT GTAAGTTCTC TGCTAGTCAG 540 GGCTGGAGAC TGCTGCTGGC AGAAACCCAA TCTTCTCCTT GCAAATAAAG GAGCCATCTG 600 ACAACGCTGT ATTTGTTGGG GCCTCTTCTG AACCAATCAG AGACTGCCCT TGACCGACGG 660 GAGGAGGAGA AGTTTATAAT AGGATCAGTT TTGTTTGCAA TTTGTTTCTA ATAGATGCCA 720 ATAAGCCAGT TAACTAGGCT CCGGTTAATG GACATTTTAT TGTTCCCCCC CTCCCGCCAT 780 GGTGCACATG ACCTTTCCTT AGAAGCATTT GTGATGCCTG AAAACATGTA TCTGCTGCCT 840 GGTAGCCAGA GGGCTTGCTC TGCTCTAGAA AACTTGTTCC CTAGCCCCGA GCTGCAGACC 900 AGACCCAAAT ACTTTGATCA TTCTGTCAGT GGGAAATTTA GAGCAACATT CGGGCTTTTG 960 TTCCATGTGT ATTTCTCCAA ATGTAATATC TCCCTCAAGA AATCAATGAT AAGCTGTTAA 1020 ACTAAAGAGC ATGGTAACAT 1040
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