Tag | Content |
---|
EnhancerAtlas ID | HS095-05484 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:64333880-64335070 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat4 | MA0518.1 | chr11:64334872-64334886 | CCCTTTCCTGGAAG | - | 7.25 | ZNF263 | MA0528.1 | chr11:64334445-64334466 | GGAGAAGGGAAGGCAAGGGGA | + | 6.34 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 64334024 | 64334364 | chr11 | 64334600 | 64335062 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I064564 | chr11 | 64332189 | 64335552 |
|
Enhancer Sequence | TTTAAAAAAC TTCAATTTTT TTCTGATAAA TCAGAAGGAG TGCTCTCACT GCAAACACCC 60 GGGACCAGTT TTTTTTTTTA AAAAAAAAAA AAACCTTCCA GGATTCCTCA GTTCTCCCAG 120 GGGCCGGCTC TGCAACCTTT GTTATTCAAA TCAGAGGCTT TGAAGCTGGT GACCTTGTGG 180 GTTTTCCTGT CTTGTTAACC CAGTTGTTAT CTGTCCAAGG CTCCAGTGTC GGCCGCTTTG 240 AGCACCAGCC CAGTGACTCT CACGTCACTC ACATAAACTT CATGAAACAC CGCGGCTTGT 300 GCGATTTTAC TCTGATGTTG TTGGGCTGGT GTTGTCCGAT GTTTATTGGG TGATGCAATC 360 AGGTGACGCC TAAGGGGAGG GCTGGGAGGA GCATCTGGGT TAAGCAGGGA GAGCACAGAT 420 TTTAAACGTG GCCGAGAAGA ATTTTACCTT GCAGCCAGTT GTGGATCCAA ATCCCATCTC 480 CAAACCATGA GAATTTAAAT ACCGTAAATT CAGCTACTCG TGAGCCAGTG GGGTGGGGGA 540 GTGGGCAGAA AGCAGACCCT GAGATGGAGA AGGGAAGGCA AGGGGAGATG CAGCCACAGC 600 CTGGGCCCAG CCCAGCCCCT GGGAGCGTGG GAGCTGGGGC CTTTCTGGGT GGTCCCTCTG 660 CCCCATGAAC CAGTCACAGG CTGCTCTCCC CAGAGAAGGG GCAGCACTCC CAGGGGCTGG 720 GGGACAGGCT CTCCATCCTG AATGTGGTCT GGGCAATGCA GCCCAGGGTC TCCCGAGAGG 780 CCCTGTCCTG CCATGATTCC CATCTTCCAA GAGAAAGGCA CAGTGTGACT GGTTATCAGA 840 ATCAAAGCCA GAGAGGGCTA GTCCGGAAGT GAGGGGCAGC TCAGAGGCCC CCGAGGGCAG 900 ACTTGGTCCC AGCCAGAGAG GCAACGCCCC AGCGCATCGC TGCCCCTGAC ACAAAGCCTG 960 TGTGTGAAGG GATGGTGGAG CCACCCTGCC TGCCCTTTCC TGGAAGAGCC TGACGCTGGG 1020 GTTGTGTCCT GAGTTTGGCA GGCTTCTGGG ATCGCTGGCC GAGACAAGCC CAGGATTGTC 1080 CTCCGGGGTT GGCCATGTCC TCCCAGGCAG CTCCTGGTGG GAGGTGCTGT TGCTGTTGGG 1140 GTGCCCTCTC CCCGGCAGGG CAGGGACCTG ACTTCCAGCC TTGCCCGCAG 1190
|