Tag | Content |
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EnhancerAtlas ID | HS175-00408 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr1:25465680-25467130 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:25467070-25467088 | GGAAGGAAGCCCGGCAGG | + | 6.35 | Foxd3 | MA0041.1 | chr1:25466199-25466211 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:25466203-25466215 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr1:25466207-25466219 | GTTTGTTTGTTT | + | 6.32 | ZNF263 | MA0528.1 | chr1:25465786-25465807 | TCCTCCCCTCCAGCCTCCCTC | - | 6.43 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I025140 | chr1 | 25466725 | 25467101 |
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Enhancer Sequence | CGATTTTCAG CCAAGCTGCT GGTGTCTTCC TCCCCTGAAG GTTCACCAAC TACAGGAGAA 60 GGAAGAGGCC TTAAAGCCCT GCAAAGGCCA TCTCTCCAGC TTCATCTCCT CCCCTCCAGC 120 CTCCCTCTCC TCTAAGGCCA ACACATAGTA CTGCTTTCCG TTCTTAGAAT GCGTCACACT 180 TTCCCTCCTT TGCAAGTGCA GTTCCCTTTG CCTGGAACAT CATTCCCTCA GTCACCTCTC 240 ACTCCCGGTC CTCTTGCTAA CTCCTACCCT TCCTGCACGC CTAGGCTTAA TCCTGGGAAA 300 CCATTTGCCA CCCCCTTCCG CAAAAAGGCA CAGGCTCCTG CTGCCAGTGC CTGGAGAGCT 360 CCTTGTGTCC CACCCCAGCC CAGAGCATGT CAAAAAGAAG AGATGAATGC CAATTTCCCA 420 TAGTGTGGTC CACTGCTTCC ATTTTTGAGG CAGAAAGTAA TGAGCAGTGG GTATCTAATG 480 TGCCCTTAAA TATCTTTTTT TGTTTTTTTT GTTTTTTTTG TTTGTTTGTT TGTTTGTTTT 540 GAGACAGGAT CTAGCTCCAT TACCCAGCCC AGATCTAGCT CTGTCCGCCG AATGGTGTGA 600 TCACAGCTCA CTGCAGCCTC AGCTTCAACT GCCTGGACTT AAGCGATCCT CCCACCTCAG 660 CCTCCTGAGA AGCTAGGACC AGAGCCATCC ACCCATGCCA AGCTAATTTT TAAATTTTTT 720 TGCAGAAACG AGGTCTCACT ATGTTGCCCA GGCTAGTCTT GAACTCCTGG GCTCAAGCGA 780 TCGTCCCACC TCAGCCTCCC AGAGTGTTGG GATTACAGGC ATGAGCCACC GTGCCTGACC 840 AAGATCTTTA AATAGTAATA AAACAGACAT TTATTAAGTG CATCTCATGT GCTGTGCGCT 900 GTTCCAAGTG CCTACACTCC CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC 960 TGCTATCATT ATCCCTTTCT CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG 1020 CTCAAGATCA CAAGTCTGGA CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG 1080 AGTCTCCCCT GGTGCCTCTC CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA 1140 AACCATGCCT GCGGCAAACT CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG 1200 TCTGAGTGAC ACTTATCTCA TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC 1260 TCCCCATGGA CAGAGGGCAG GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG 1320 GGTCCAAAGG TGCCGTCTGG CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC 1380 ACAGGGACAG GGAAGGAAGC CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA 1440 TCCAGGGACA 1450
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