| Tag | Content |
|---|
EnhancerAtlas ID | HS087-16940 | Organism | Homo sapiens | Tissue/cell | HEK293T | Coordinate | chr6:7672480-7674030 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr6:7673681-7673692 | AGCTGTGATTT | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 7672507 | 7672800 | | chr6 | 7673000 | 7673200 | | chr6 | 7673200 | 7673441 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH06I007670 | chr6 | 7670816 | 7673995 |
| Enhancer Sequence | AATAACATGA TTGTGTGCAC AGGGTCAATT GCAGTTCAGA TGAGAATTTA CCGCTGCTGA 60
GCTGCAAATG GATAAAGACA GAGAGAGCTG CTGTTAACCC CTTATTAACA CAGCCCAAAT 120
GCCTTTCTTT AAAGGAAAAC TTAGACCAAA AGCTCCTTGA GGCCAGGAAA GATGTCTTCA 180
ATATCTTTAG ATATTTCCCC ACCTCCAGTG CGGGTCCCGG TGGTTGGCAC ACAGTAGCTG 240
TTCAAGTGAA TGAACGAATC ACTTTTGATC AAAAGAAGAA GCAGGGCTTG TTTTTCAAAT 300
TGAGAAATGG GAGTGGTTGT ATTGTAGCTG CATTGTTGAG TCTCCTGTGT GCCACGTGAT 360
CCAGCAGGAG AATCATAACC GGGCTGAGCC CACTCTCTCC CATGCTGACA GTGCTCTTAG 420
CAGCCGCGGC CACAACACGA CCTCAGTGAC AGCAGCCACG GCGGGCCAGG ATCTGTGCTA 480
AGGGTTTTCC ATGCCTCCGT TGCACGTACC CTAACAACCA CCCAAGGAGG GGGTGTTGTC 540
TTTGTATCCC AGAACGGTTA AGCAGCTTAC TTGGGATCAC ACAGTAAGTA GCGTGGCAAG 600
AACTTGCACT CAAGCTTGTC TGAGTCCAAG AGCCACCCCA GCACACTGCT CACCATGGTC 660
TTCCCAAAGG GATCGGGCTT ATTCAGAAAG CCGATCAATT GGAAGGACCA CGTAGTCACC 720
GTAGAAGAGC TTGGGAAGAG TGTCAGGCAG TCTCAGGGGT ATTTAGGGTC TCCAGGGTCC 780
ACTCCCTGGC ATTCCTGGAG GGCTCTAGTG AAAGCGTGAT TATCCCGGGC AGCCTTCAGC 840
AGTGGAACAG CAGGGAACGC CAGGGTTAGG AAAAGCCGTG GGAGGGAGGA AGAAGCTGGA 900
AGGGAGGGCA TGCCCGCCTG AAGCCTGAGT AGCCTCGGGG TGTGCAGGGG TGGGGAGTGG 960
TGTTTTGGAC GCCGGCCTGG CCCCACCCTG CTGACTGCCC CTGTGGGAGG AGGGTGGGGC 1020
CGTGAAGGGA GGGTTGTTTA TAAGCACCTC TGGCCTTTGA AAAACACCAG CTGATGGCGC 1080
CACTTCCTTC GCTTCTAGTG TAAGGCCCCT CGGAGTCAGT GTCACTCCAG CCACCTGCAG 1140
TCCCCAGCCC GGGCTGGGGC GGAAACGCAG GGCAGCAGAA TGAGCGCGGG TTTTGAAATC 1200
CAGCTGTGAT TTGGACCAGC TGTGGGCAGA TTACTTAATA GCTCTGTATC CTTCTTGGGA 1260
GTAATAATAC CCACCTTATG CAGTTCTTGT GAGAATCAAA ATGAGTCCAA GCATGTGAAA 1320
TATTTAATGC CTGGCATTTG AGAAATGTTC AATAGTAGTT TCTATTCCAA ACTCGCCCAT 1380
CCTCAGCCCA CAGTCAGGGT GGCTGTTCCC CATTGTAACC CTCTTGAGTG CATTACTGAT 1440
ATGCTCTAGG GTATGCTTGA GAGAGGATAT GGGAATTTTC CTTCCACTCT TCACCTAGGT 1500
TTTTACATAT GATCCTTATT TGTGGAGTGG TAGCAGTAAA TCCTTGAGGG 1550
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