Tag | Content |
---|
EnhancerAtlas ID | HS014-00248 |
Organism | Homo sapiens |
Tissue/cell | CCRF-CEM |
Coordinate | chr1:149781100-149783430 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr1:149782649-149782660 | AAGAGGATTAA | + | 6.14 | EWSR1-FLI1 | MA0149.1 | chr1:149783191-149783209 | GCCTCCTTCCCTCCATCC | - | 6.3 | EWSR1-FLI1 | MA0149.1 | chr1:149783195-149783213 | CCTTCCCTCCATCCCTCC | - | 6.57 | ZNF263 | MA0528.1 | chr1:149783191-149783212 | GCCTCCTTCCCTCCATCCCTC | - | 6.12 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGTCAACAA ACTTTCATTG AGAAGCTATT TTATAGTAGG CATTGGGATA GCCTTTGTGG 60 AATAAATACC GAGAAGCATA TGTCTCTAGC AGAAGACAGA CAAGAAAATG TAAAAACAAG 120 AAAAAGAAAT TGAGGAATAA GCCTACAGTT TAAAAAGCTA CACAATTATT CGTTATGCAA 180 GGAATGAGGC CTTAAGAGAA AGACTTCCCT GTGAACTACA ATGAGATGAA AAAGCTTCTC 240 AGAGTGAGAT TTGAGCAAGA GTTTAAAAGA ACTGACAGAC TGATAAAAAG CTTCAAGTAG 300 TCCAGAGGAC TGAGTACTAA AACTCAGAAC AATGTAACAA AAGCACAGAA GACAAAGTTA 360 AAATGCTTTA CATGACAGTA GAACATTTAG GCTAAGCTGG AGGACTGGGG AGAACAAGTG 420 AAGAAGGTAA GTTTTGGCTA GATAATAGGT GGCCTTTAGT GTCAGGATGA GGATTTGGAA 480 GTTAATCTTT TGGTCAGTGG ATAATAAATG ATGGCATTTG TGTAGTTGAG CCAGTTGACA 540 ATGCTTTAAC AACTTCAAAA GGCCCTGAAA AACATGGTCC CTAATCCTTA AGAAAAAAGG 600 AACTCCTGAC TTCAGGACCC TAAGCTAGGA GGAAATTGGA TAAATTCTCT TATGGCCCAA 660 CTGTATAGAA AATAGACCAC CTCGGCCGTC TCACTTACTG AGTAACCTTT CCTACCAGAG 720 AATGTGCTAT ATATGATTTC TTTACTTTCA ACGGAAATTT TGGATTCTCA GTTATCTTTC 780 CCTGACCTCT TGTCTGGTGA TCAGAAAAAG ATGACTAAAC TGGGAATCTT TATTTTCTAG 840 TGGAAAAAAA AAATCATGTA TACCGCATTT TATATCTTTT AATTGGGTGT AAATTTGAAT 900 TTCAACATCA TAAAAATTAG TAAAATTCAT TTTAAGCACA AAGTTGTTAA TTCCCCCAAG 960 ATTTATCAAG AATGGCTTAA TTTCAAAGGC TGTCAAGTTA ATTATAAGCT AAGATTTTCC 1020 AGTTGCACCA AGGGTATATT TTATTTGGCA AAAGAAACAT CCACTGGCTT TTGTCAGGAT 1080 GAGTCTTGAG TTATTCAAGT TTTGAACTGA GAGGTCTTCA GAAATTCACC CCACATATTA 1140 ACTGTGGCCT TCTCTACACC ACAAATTCCC CTCCACTCAT CCTCAAATTG TTTCCTTTCT 1200 CAGGACATCT GTGACACAAA GACTGTGACA CACCCACAGG TCGATTAACA TGAGGACCCA 1260 ACACCTATTA AAACATCCAC ACTCCTGAGA ACACTAAAAA CCAACCACCT CGTCAGGTCC 1320 CACCTCCAGT CTAGCTGAAT CAGGAAACCT CAGGAGAAGC ACCTGGAAGC AGGTTTAACA 1380 AGCGCAAAGG TGACTCTTAT AATTGGGAAA GTTTGGAACC AAGACAGGGT TCTTGTCCTG 1440 GAGGAAGTAT TTTCCTGTGG AGAAGGACCT GTAAACAGCC TATGAAGTGC TCAGCTTTCA 1500 CCAAGAAAAG AAAAACATGG GCTGATAGGG TTAAGGAAAC GTTTGACTGA AGAGGATTAA 1560 ATCCTGAAGG TTAGGGATGT CTTTGGGCGC TGGGGTCTCT CAATCACCAA AGATCGACAT 1620 TACAGGCCAG GTAGCTCTTT GTCCCCCCAG AGGACTGTCC TGTGCCTTAT GCTTAGCACT 1680 CCTGGCCTCT GCCCATTGGA TACTTCTAGC ACCTCCCCCG CAACACACAC ACACCTGACA 1740 ACCCAAAACA TCTACAGATA TTGCCAAATA CTCCACAGGG GGTGGGGTGG TGGCAATATA 1800 TCTCCCTGTT TGAAGTCACT GGAATGGAAG TTAGGGGAGG ATGGCTAAGT CAGGACTTGC 1860 AAAAAGGCTA AGGGACGAAA GCACATGGCT ATATTAGACA AAGTTTGTGA CAGACGCCTG 1920 TAGGTATATG GTAAGGAAAA CAGATTAAAA CACTAAGAAA TAGTAAGAGG TCGGACCGAG 1980 GGTTTCTCAT CTGTATGGGA AATCTCATCT CGTTCATTAC TTTCAGAAAC AAAAAGGAAA 2040 ACGACTTTAA AGATACAGGT TAAAGGCCGA AGGGGTGTAG AACCACCCCC CGCCTCCTTC 2100 CCTCCATCCC TCCCAAATAT CCCAGAACGA GTCAAACCTT TCGAATCTCG TAGCACAGAT 2160 AACAAGCAAC TCAGTAAGAC TGGACGGGGA TGACTGAGGG CCAACTCATT ACAGGACTAC 2220 AGGAAACTCC TTAGTCCTAA ACCCGAATGC ATCCGTGACC ATGGTAACAC TCCCTACCTG 2280 ACCAAAAGCT ATCAAACGCT CTGACAAGTG TTTACAGCTG CTTTCTCGAT 2330
|