Tag | Content |
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EnhancerAtlas ID | HS098-48146 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:31093620-31095270 |
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 | chr6:31094278-31094296 | CTTTCCTTCCTTCTTCCC | - | 7.46 | SNAI2 | MA0745.2 | chr6:31094803-31094813 | TGCACCTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr6:31094544-31094565 | CTTTCTTCCCCCCGCTCCCCT | - | 6.05 | ZNF263 | MA0528.1 | chr6:31094273-31094294 | TCTACCTTTCCTTCCTTCTTC | - | 6.09 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr6 | 31095087 | 31095270 | chr6 | 31093704 | 31094128 | chr6 | 31094589 | 31094950 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I031124 | chr6 | 31092670 | 31095269 |
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Enhancer Sequence | GTTCACTGAG TTCCCAGCAC ATAGCTGTGG CAGGCACTTG GTGATATTTT GAAATAAAAG 60 AATGGAAGAA TGTGTCCAGG CTGTGCTTCC CCTTTCTACC TTACTCAGGG ACATGGTGCC 120 CTCCTCTCTG GTTTCCTGCC CTGTGCCCAC CCCCCACCCC CTGCAAGCAC AGCTCTTATG 180 TGCAAAGCCC CTGTAGGTGC TGGAGGGATT CACTGATGGC CTTGGCGGAG GTGGCAGTGG 240 GCATGTGCAC TTGGCTCTGA CACAGCCACT CATGCAACAC CCTGTGCAAT CTCGGCCTGG 300 GCCTGTGTGT CCTGCCCTCA TTCCTCACGG GTGACTGTCT CCCCTGAGCC ACTCTTCTCT 360 CTATTGGATT AGCTCCTTTT ATTTCCCCCT AGGGATGCAA CACATTTTTA TGAACAAACA 420 GCAGTGTTCA CATGGCTGTG ATGAGGACGT ACTGGGGTTT CCCCTGGACA TGGCATTCAT 480 CTGATGCCAG TGGTGGGCAG GACCGTGCTG TATACTTTAA AAAAACCCTA GGGGGTTCTG 540 TTAGGTGCCC CCACTGCAGC ATAACGAGTT GCCCCTAGCT GAGAAGCCCT GTCCTGGGGC 600 CTGTCCACAC CATCCTCTTC CTGAGATTAT TCCTGGTGTG GGCGGTGCTC GGCTCTACCT 660 TTCCTTCCTT CTTCCCTGCT TGGCTCCTGG TCCAATGGCT CTCTCCTCTA TGGAATGGCC 720 TCCTGGAGCT TGGCTGGGTC AGCCCCCACT TTCCACTCTT CCCATGCCTG TCCTCACCCT 780 CCCAGCAGCC CTGCCAGCCT CCGACGGGCC CAGGGCACTG CAGCCGGCAC TTGGGAGTGA 840 AGACTGGGGC CAGAGCCAGG CTCACCTTTG GCCACTGAAT CCTGAAAGAG GAGGAATTTG 900 GCAAGTGGGG TTCTGCCCAC CAAGCTTTCT TCCCCCCGCT CCCCTGAGTC TTTTCCCTTC 960 ACCCCCACTT CCCAAAAGCA GCAGGGAGTC AGCTGTAGGG CAGTCGCTCC CTGGCCGAAG 1020 CCTTCCTGGC TGTTTCCGTC ACACCCTGAG GCCACCCCTC TTATCTTGCG AGGAGGGAGG 1080 CACACAGAGG CTGTGATTAG CTGTCACAGT AGCAAGACTG TTCCCCTCTC TGTCCTGCGG 1140 AGTGAGTGTG AGGGAAAAGA GCTCTCCTTG TCTGCTCATT ATGTGCACCT GTTAAATAGT 1200 CATTCTTTCC ACTAGGGCTA TTAGTGGTTT TTATTGTTAC TGGTCACCCA GAATTAGAGT 1260 CACAGCTTCC TCGACAGGGT GAAAGAGAGC GCCAGGGTGC AGTCTGAACG TGCTCTCGGG 1320 AGAGGAGAGG CCGGAAAGAC TTGTACCAGG AGGGACTTCT AGGCTGGGCT GGCCCTTGGA 1380 GCGCCTAGGA ATGGGACTGT GGTGGCCCAT CTTCCCTCCT GTGTTCTGGG CTGTCTGAGT 1440 GCCTCTGGGT GAGAGTCCTC ACAGGAGGGA GCTTCTCCTA CTGCCCAGTG TCTCCCTGGC 1500 ACCTGAGGCA TCACCCAGCA CACAGAGGTG ACCAGGAAAC ACAGACTCCT GTTAGAGAGG 1560 CATCTCGTGT CCCGCTCTGT TCTCTTGGGC CCTGGGACTA GAACATCTTC ACCAGAGACC 1620 GGCGCCGACT CCTTGGCAGT GTGTAACATT 1650
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