| Tag | Content |
|---|
EnhancerAtlas ID | HS183-09369 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr7:38766580-38768140 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr7:38767335-38767346 | TAAGTAAACAT | + | 6.02 | | Foxa2 | MA0047.2 | chr7:38767333-38767345 | CCTAAGTAAACA | - | 7.22 | | NFIC | MA0161.2 | chr7:38767516-38767527 | TCTGCCAAGAA | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGCTGCATCT GGCGAGGAGG GCAGAGAAAG GAGGAGAACT TAATGCAACA AGCAAGATCA 60
TTTTAAACCA ATCCCGACTG AAAGTCGAGT TGCAGTTTAA TTTTCAGCAA TAAGGTGCCT 120
TTAGAGAATG GCTTATTTAC AAAAGCATTC CTGAGGGGTG GTATGATCAG ACACAAAACA 180
GGTATTATAA TCATGTTGCT ATGCGATTCA CAGGTTACTT GCTTAGCCTC TGTGTCACTT 240
ACCCAGACTA CATTGAGGAC AACTGTAGGA AAACCAGCAA GTGTATGTGC CAATGCGCCC 300
CTAACCCCTA TAATCATTAT ACACCACAGC TGAAGTTGAG TCTGTGGCTT CATAAAAATG 360
CTTTGCCAGT CCACCTGCTA CCTTTGCCAA GACCACACAC TGACTCAGAG GCGGACCTGG 420
GTTACAAGCC CAGGCTGTGG TGACCTTGCA TTTTACTGCA CTTGTGCTTG GGCAGATCCC 480
CTCATCTGTT CCTGCTCTGT GTGGCCAGCT TATTTTTGGT AAGATTTAGT GTCATCAGCA 540
GAGTAAATTT GGAGTTAAAT CTAACTGTAG AGTGGGAATG TATGTGGTTC CTTTTTGCTG 600
CAACACTGTC TGAAATGCTA TGGAAGCTCA CTTCTTCACC TGAGCCCATG CAGTTTTCAA 660
CAGAAGCACT TAAACATCCA AATCTAATTC CTCTAGAAAA GAACCTAAGT AGAACAACTT 720
CTCATGGACT GCCCCATGAA ATAATCCTTT AATCCTAAGT AAACATGAGG TCAACTAGGT 780
CTTTTAGTAC TTTGTTATGC TGAACTTATA TTTGAAAAGC ATTTGTTAGC ATCCTAACAA 840
TGCTTTGTTA GTTTCCGCTT TTGAATTATG CAAATTTCTT CTGTCATAAT AAACCTTAAG 900
AAGGTGCTTT TCATTACAGA TGAAGACATA TATCTATCTG CCAAGAACTA GAAATAAACA 960
AATGCTTATG TCTTTTAAAG ACTCACAGTT CCAATTAGAT GGCAGGGATT ATGTATGTTT 1020
CCACTGAAAT GTGAGATGAC TTGGGCATGT AGAACCATAT ATCAGAGAAA AACACTAAAG 1080
AAAAGGGAAT GCTACCTATA AATTTTTTTT CCCAGACATG TATATGGTTC TTCTACCTTG 1140
AAATTTAAAT GCTGATGGTT AGTTTTCATT TTGTTTTTAC CCTAGACTAG CAGTTCTAAA 1200
AGAAGGGCCC CTGAACCAGT GGCATCAACA TTACCTGGGA ACTTGTTAGA AATATACATT 1260
CTCAGTTCCT GCCCTGGAAG TTTGGAACCA GAGACTCTAG GGAGTCTGAC TGGGTCAGCG 1320
ATCTGGGTTC CAATAAGCCT GCCAGGTGAC GATGACTCAC CCTAGAGCTT GAGAACCTCA 1380
GCTCTAAGCA ATGGCAGCAC CAGCATTCCA CTGAGCAGGA TGGAAGCCAC AACACTTCTC 1440
TCCACTGGGT TATTCTGAAA GTTATATAGT TTTATAAACG GTAGTTGGCT AATTCCAAAA 1500
TTTTGATTCC ACTCATCATT AAAATACATG TTTGGGATTT TTTTGGGGAA AACCTTCTTA 1560
|
