Tag | Content |
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EnhancerAtlas ID | HS165-00469 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr1:56898000-56899370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr1:56898488-56898499 | TGTGGATTGGA | - | 6.62 | REST | MA0138.2 | chr1:56899235-56899256 | CCCAGCACTCAGGACAGTGCC | + | 6.6 | ZNF263 | MA0528.1 | chr1:56898614-56898635 | TCCTCTACCCACTGCTCCCCC | - | 6.12 | ZNF263 | MA0528.1 | chr1:56898611-56898632 | TCCTCCTCTACCCACTGCTCC | - | 6.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I056432 | chr1 | 56898273 | 56898672 |
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Enhancer Sequence | ACTGGCGGTA AAGACTAAAT GGGACCTCAT GTATCAACAT GCCTAGCATG ATCCTAACAC 60 ACCAGGAGCT TTCAATGCTC CCTCCCTTCC CCGATGGCCC AGAAAGGCCC AGAAAGCCTA 120 ATTCCTTTCA GGGAACCAGA GAGACGAGAC AGCACAGGTA TAGGGCTTAA GGAGGGCAAG 180 AGTGATTTCT GTGTTGGTGG TGTTTTTAAA TGCTAACTGG AACAGGAAAA AAAAAATCAG 240 GTGAGAGAGA AACCACAATG CCTGCCAAGG AGTAGCCTGC ATTGTTCGCC CCTGGAAAAG 300 CTGCTGGCTT AGGGCTTTTA AAGCTGGGGA AAGGTCAACC CCTCGCAAAA GAACAAACTG 360 CATGGCCCTG TGACTTCCCT CCTCTAATTC CCATAACTCC CTGTGCTGGT TGCCTCCTCT 420 GGAACGTGGG AAGGTGATCC CTGCCCTGCC AGGGCTGTTT GGGCTGTGTG CTTGTGCTTG 480 CAGGGCTTTG TGGATTGGAA AGTGTAGGCA ACCTGATGAA GAGGGTTGTT TCTGTGTGCT 540 TAGCTCTGCC AGCCTGGCCT CCTGACCTCC CATGCTGTTT GCTCAGCGCT ACCCATGTAC 600 CTTCCCTCAG GTCCTCCTCT ACCCACTGCT CCCCCTTCTT GATTTCACCT TCCAAATCCT 660 CCCATCCTTG ATAACTGCAT TTCCAAGAAG CCCCTGCTGG TGATGTCGGT CTGCACTGAC 720 CTCATGCCCT CAAGATGTCT TCAGACTGGA TGGCACCATG AGAGTCGCTT TCTTTCTTCT 780 GTGTTTTGTT TTCTTTTCCT GTTGTTTTTT TCTCACCTCT CTCAGCAAGG ACCACCTGGT 840 CTCCCACTTC CCCCATATTA TCATTCTCAG AGGGCCTCCC CCAATCTGCC CTCACCCCCA 900 CCTGTTCCGA ATCTAGCCAC ACTTTCATGC CCCAGTCAAG GCCACTCCAT CTGTGTGCAC 960 CAACCTGACA ATTTCAGTTC CCCAAATGTG CCATGCTCTA GCTTTCCTTC CTCATCTTCC 1020 TACTTCAGGT CTCAGTTTAG ATGTCACCTC CTTGATCCTC ACCTCCAATT CCGCTCAGAT 1080 GAGGTGCCAC TGCTATGAGT TCCCTTGACA CCCTGTGTTT CCCCCATGAC TGCACTGATT 1140 CCTGCTGAAA TTAACCAGTC TATGCCTTTC TCCGGCTCTT GCAAGAAACT GTATGTGAGC 1200 CAGGGCTTGT CTCTCCCATT CTTTAGAGAG AGATCCCCAG CACTCAGGAC AGTGCCTCCC 1260 CAGGGCAGCT GCATGAATGG CCTACCGTGG ATTATCCTAC TCTCTACTGC TTCACCCAGC 1320 ACCGAACTCA TAACAAATGC ACAACAGACA TTATCATGGA CCCATTCTGT 1370
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