Tag | Content |
---|
EnhancerAtlas ID | HS042-01665 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:53968180-53971900 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:53970293-53970308 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr1:53968485-53968506 | AGGGGAGGGGCAGGGAGAGAG | + | 6.01 | ZNF263 | MA0528.1 | chr1:53968504-53968525 | AGGGGAGGGGCAGGGAGAGAG | + | 6.01 | ZNF263 | MA0528.1 | chr1:53969786-53969807 | AGTGGAGGAGGGGATGAGGGG | + | 6.06 | ZNF263 | MA0528.1 | chr1:53968393-53968414 | GGGGCAGGGAGAGAGGAGAGG | + | 6.14 | ZNF263 | MA0528.1 | chr1:53968418-53968439 | GGGGCAGGGAGAGAGGAGAGG | + | 6.14 | ZNF263 | MA0528.1 | chr1:53968429-53968450 | AGAGGAGAGGGGAGAGGGGCA | + | 6.14 | ZNF263 | MA0528.1 | chr1:53968184-53968205 | GAGAGAGGAGAAGGGGGAGGG | + | 6.29 | ZNF263 | MA0528.1 | chr1:53968476-53968497 | AGAGGAGAGAGGGGAGGGGCA | + | 6.35 | ZNF263 | MA0528.1 | chr1:53968187-53968208 | AGAGGAGAAGGGGGAGGGACA | + | 6.44 | ZNF263 | MA0528.1 | chr1:53968603-53968624 | GGGGCAGGGAGAGAGAGGGGA | + | 6.67 | ZNF263 | MA0528.1 | chr1:53968363-53968384 | GGGGGAGGGACAGAGAGAGGA | + | 6.74 | ZNF263 | MA0528.1 | chr1:53968491-53968512 | GGGGCAGGGAGAGAGGGGAGG | + | 6.79 | ZNF263 | MA0528.1 | chr1:53968510-53968531 | GGGGCAGGGAGAGAGGGGAGG | + | 6.79 | ZNF263 | MA0528.1 | chr1:53968229-53968250 | GAAAGAGGAGAGGGGGGAGGG | + | 7.01 | ZNF263 | MA0528.1 | chr1:53968693-53968714 | GGAGGAGGGACAGAGAGGAGA | + | 7.01 | ZNF263 | MA0528.1 | chr1:53968232-53968253 | AGAGGAGAGGGGGGAGGGAGA | + | 7.72 | ZNF263 | MA0528.1 | chr1:53968690-53968711 | GGAGGAGGAGGGACAGAGAGG | + | 7.72 | ZNF263 | MA0528.1 | chr1:53968241-53968262 | GGGGGAGGGAGAGGGAGAGAA | + | 7.96 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33491 | chr1:53968320-53969790 | H2171 |
|
| 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 |
GH01I053502 | chr1 | 53968401 | 53968530 |
|
Enhancer Sequence | TGGGGAGAGA GGAGAAGGGG GAGGGACAGG GAGTAGGGCG AGGGACAGGG AAAGAGGAGA 60 GGGGGGAGGG AGAGGGAGAG AAGAGAGGGG AGGGGGCAGA TAGAGAAGAG AGGGGAGAGA 120 GGCAGATAGA GCGGGGAGGG GGAGAGACAG AGAGGGGAGC GGGAGGGGCA GGCAGAGATG 180 AGAGGGGGAG GGACAGAGAG AGGAGAGTGG GGAGGGGCAG GGAGAGAGGA GAGGGAAGGG 240 GGCAGGGAGA GAGGAGAGGG GAGAGGGGCA GATAGAGAGG AGGGGGGAGG GACCAGAGAG 300 GAGAGAGGGG AGGGGCAGGG AGAGAGGGGA GGGGCAGGGA GAGAGGGGAG GGGCAAGGAG 360 AGAGGAGATG GGGAGGGATA GAGAGAGGAG AGCGGGGAGA GGCAGGGAGA CAGGAGAGGG 420 GAGGGGGCAG GGAGAGAGAG GGGAGAGGGG CGGATAGAGA GGAAACGGGG AGGGACAGGG 480 AGAGAGGAGG GGGGAAGGGA CAGAGAGAGA GGAGGAGGAG GGACAGAGAG GAGAGTGGGG 540 AGGGACAGAG AGAGAGAGAG GAGTGGGGAG GGACAGAGAG GGAAGGGCGG GACAGGGAGA 600 GAGAGGGCCC TGATCCCTGA TGGAGACAGA GAGACCAAGG CTTCAGGGTG GGGGTGCTGG 660 GCCAATCTAG CTTGAACTTG ACAGAGGCCA GGACTGTGGG GGCGGCCTGG AGTGGCAGGG 720 CTGGAAGGAT GCCATGGTCT CCTGTCCATC CTGGGCTCTG TGCCTATGCC CTGGGTTGGA 780 CTCGGGGGCC CCTGGGTGGA CTCAGCCCCT TGGCTCTATA GACCCTGTGG GGTCCTGGGC 840 TTGTGGCCCC CTAGGGGCTC TCTAGGCCCT GTGAGAAATC TCAGCCCCTC CACCTAACCC 900 CACTAGCCTC CCTGTGTGAC AGTGACAGTC ACACCTCCTT GCCAATGGTG GGTCTGGGGG 960 TAATCGCCGT GCCCTGCAGT GGCAGTGGCC AGGCTCCCAT GTGCTGCGGG CTGCAGATCA 1020 GGGCTTGGGA GGGGCTTTGG TCTTGGTGTT TTTAAAATAA GGGCTGAAGA TAGCACTACG 1080 GAGGGAGCTC AGGTCCAGCC CCCGGGGGTC CTGCCTGGGG ACCGGTGTTG CAGTGCTCGC 1140 CTTCGCCTTC GATTAGGAGG GAGACCCTGC CGGCGTCGGG GCAGGGCGTC CCGAGTGTGC 1200 CAGGAGGAGC GGGGGCTCAG TGGAGTCCCA GGCAGAAGAG TGAGGAATGG CATTTCCAGA 1260 TCCCGGTCAC CACAGCAGTG GGACCCACCC CCGAGCCCCT CCGTGCCCTG CCATCCCCTG 1320 CGGCCTACTT GTCTCTGCTC TGTCTCGGCC TCTTTGTTTC TCTGCCTTTG TCTCCTTTTC 1380 TCCCTCTCTC TGCTCTCTGA AATTAAATGG GATCCAACTG CCAGCTCCCT GTGTGTTCCC 1440 CGCTTGCGGC TCAGCCCCTT TCATTATTAA CAGAAATATG TCCTCATGGT GGAGCTTCAC 1500 GCTGCTTATC TGGAGTGGAT TAAGTGTTCA CAGTGACATG CAGTACTGAT TCCTCAGCAT 1560 CCCTGTTCAA GGAGTTTTGC CTCGGCCTAA TTAGTTCCAT AAAATCAGTG GAGGAGGGGA 1620 TGAGGGGCGA GGGGACCCTG GGTGGCAGGC AGCAGCCCGA TGTGCTGTGT GACAATGGGT 1680 CGATCCCTCC CTGCTGGAGA ATTGGACTGG GCCACTCTGG GAGGCAGAGG CTGAGAGGTG 1740 GTGGGAGCAG GTCGCCCGAT TCTGCAAGGG GCAAGACAGT CTGAAGGGTG AAGGTGGAGG 1800 CTCCGGAGCC CGATGCCCGG GTTTGAACCC AGCTCTACCA CTCACAGGCT GTGTCACGTG 1860 GGCAAGTTCC TTAACTTCAC TGTCCCTCTT TTTTTTTTTT TTTTTTTTTT TGAGATGGAG 1920 TCTTGCTCTG TCACCCAGGC TGGAGTGCAG TGGCGCGATC TCGGCTCACT GCAACCTCCG 1980 CCTCTCGGGT TCATGCCATT CTCCTGCCTC AGCCTCCAGA ATGGCTGGGA TTACAGGCGA 2040 CCGCCACCAT CCCTGGTTAA TTTTTTGTAT TTTTAGTAGA GACAGGGTTT CACCATGTTG 2100 GCCAGGCTGC TCTTGAACTC CTGACCTCAG GTGATCCACC CGCCTTGGCC TCCCAAAGTG 2160 CTGGGATTAC AGGCGTGAGC CACCGCGCTG GGCGCACTGT CCCTCAGTTT CCGTGCCTGT 2220 AGGATGGGAG TAAGTAGCAG GGTTTGGCAG GGAAGACCGT CCTTTTCAGC TCAGGGTGGT 2280 CAGGAGTTTC CTGAGGGGAC CATGCTGCGG TGTGGGCCGG GGTGTCTTGA GTGATTCCCC 2340 AGCCCCACCC CACGCCGAGT GAGGGAGGAG AGGAGCAGCT CCCAGTCTGG AGTGGGCTGT 2400 GTGGAGAGAG CCACTGGACT GGGCCGAGAC CTTCAGTGGA AGACACAGCC ACCCAGGGAC 2460 CTTCCCTCCC ACCTCCCTCC CATGCTGGGC TCCTCACTGG CTGGAGCCAG CCCGGAGCCA 2520 GAGGGCAGCG GCCCTAAATG CAGCCCCCAC AGGTGGGCCC TGGACACAGA GCAGGCAGAG 2580 CGCATGTCTG GAGGGGGCAA GTAGGACATG GGTGCAAGAA CCTCGTCAGC AGGCTCCTGG 2640 GAGGAGGCAG AGAGCAGATC CCCGGGAAGC CCTGCAGGCT GGCATGGCAC TGCTGTGTCA 2700 GTGGCATCGT GGATGATGGG GAGGACCAGG CGCTCATCAC GGCTCTGTCA CTATGTGGCT 2760 AGGTGTTCAC TCTGACCCTC AGTCTCCCTC TCTATAAAGA AAGGGGTTAC TGGGCCTTTC 2820 ATCTTGTTTT GCCTGCCGAA GTCAGCGTGT AATACAAAGA GGCGGCCCTT TGGTGAGGGT 2880 GTGAATGCCG GCTGCCCCTC CTCACCTACA GAGGAGACAA GAAGACCCCT CCCTAGGCTG 2940 TTTCTGGGAG CACCGGGAGG GTGGTAAACA TGACCGCCCT TGCATGGTTC CACTCCAGAG 3000 GGGATGAGGC AGGAATTTTC CTGGATCTTT GTAGCAGGTG ATCAGTGTGA CACGGTGAGA 3060 TGCTGGCCAT CGTCCAGGTC ACCTGCCCAG GCCTGGAGCA TGGGCCTGTT CCTCGTGCTG 3120 GATGCTGGAG AGCGAGACGG GGAGATGGGG ACAGACCCAC GCAAGCCTCG GTCCTCCAGG 3180 GTGGGCACAG GGCTTCTGGG ACAAAGGCTG CTCTTGGCAC CTGGCCTGTC TGCAGGGACC 3240 AGCCTTTGCC CTGGCTTTTT GAGGCTGTTT GGGCTCCATC CCCAGCAAGC TTGCCCTGCC 3300 CTCCCAGTTT TCTCTGTTTG CAGAAGCCCA GACACTAGAT TTGAAGCTCG TTCTCCCACC 3360 CGCTGAGGAG TCGCTGTAGC AGGTAGAGGC CCAGGTCAGA CGGAGCTGGG TCCCAACTGT 3420 GGTCTGACTG TGGGGCCCGG GATCTGAAGC CCGTCGCCGC ACCCTCCCAG CCTCAGTTTG 3480 CCCACCTGTC CATGGGGATG GGCCTACCTC ACTGCACAGT CCTGGGACTA GCGCTGGTGT 3540 CTGTAAGGAC CATAGCGCAT GGTGGGGGCC ACGTGCCACT GGTTCCCATC CTCGTGGTCA 3600 GAACCCAGGG CCTGAGCTGG TTTCTACGCA GCCTCCCTAG CCCTGAACAC CTGGCTCTGT 3660 CACCCTCCTC CGAGGCTCTC CCGGTCCCAG CCTCTGGGCT GAATCATAAA GCAGAACGAG 3720
|