Tag | Content |
---|
EnhancerAtlas ID | HS053-23578 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr2:240551870-240553230 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr2:240552348-240552359 | AAAACAAAGAA | + | 6.62 |
| | 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 |
GH02I239629 | chr2 | 240551657 | 240553370 |
| Enhancer Sequence | GTTTCTTTTC CCCAGTGCCG CCTCCTCCAG CCTCCAATGG AGGTGTTTCC ATGGGTGACC 60 ACATTCTGTT CCACTGGTGG TGGCCTTTGT GTGAGTGCTC CTTCAGGGAC CACATTGATC 120 ATTAACACAC CTTTGAGGTT TCTTTCTTTT TTCTCTGAAA CATGGCTTCT TAAAAACTTT 180 ACACTTTTTC TCTCATGAGC ATTTTAACAC ATTTAAAAAA TAACAGAACA GTTAAAAAAA 240 AAAACCCACA GTTTCACACA GGCTTCTTCT CACTGAATCA TGTTTCATCT TTTCCCTTGG 300 CACAACCAAA GGGAAGGTTA ATTTAAAACA GCTGAGAGTG ATGTCACGTC ACACGCCGAC 360 ACCTCTTTTT CTTTTTTTTT TTTTTTTTTT TTTTTTGCCA GGAAAGAAAA GAGGTTCACC 420 TCAGGCTGCT CAGAAGGAAG GTGTTCCAGG AAGGCCAGAA AAGGGAGGCT GCTCTGGAAA 480 AACAAAGAAG AGCTTGGCAG GTCCTAGAAC GGAGGAGAAG TTAGACCCTG GGAATCCAAG 540 ATGCTGCAAC GTCAGGCAGC TGGTCCCCAG CAAGGCTGGC ACGTGGAAAC CTCACGGAGA 600 AAAGTGATTC ATAACCAAAG CAGGGCTCCC ACAGCGACGC TGAGCAGACA CAGAACTATT 660 TTTCACATAA CACTTATTTT ATTTAAAAAA AATGTTAAAT GACTTTCCTT TGCATGGATT 720 CTCTGTTTCT CTTGCTCTGG TTCTGGAAGC CATGTGGAGT GGTGGCCAAG AGTCAGTCCT 780 GTTCTGTATT TTTTTGTTGT TGTTGTTATC TTTCTGAGTT GATCAGCAAC TGAGAGAATT 840 GAGGAAAGTC GCCCAGGTGG CTCATGTCCA GTGCGTCACT CCACCCCATT CCGACAGCCT 900 CATAGGTTGC TTAACTCTGG AGCCTGGCAT TCTCCAGATG CCCCTGCAGG GAGGATTACT 960 TGGCTCCCTC CAGCAGACAA CCTTGTGGAA CGCTCAGAGC AGAAGTGAGT CACTGCAGCA 1020 GGCCCTGTGC ACGGAGGCAA GCCAGGAGGT GGTGGAGCTT TATGCGTCCA TCATCAGCAT 1080 TAAAGATGCA GCGAGGGGCA GGGCTCCTTC CCCCAGAACC ATGCATGGTG GGCTATTTGT 1140 CCCCAAGTGT GATCTTTGCC TGCAAGGTTC CTGCTGTTGT GGCACTCAGA CCTTCATCTA 1200 TACCTTCCTC AGGAATTCTG TAAACTACCA AATAGTTTTA TCAATAACCC CTTCCTACCT 1260 AAGCCAGCTA GAGTGAATAC TTAAGGCTGC ATCTAAGAAC GGTGACCAAT TTAATCACTT 1320 CACTAATTTT AACAATGGCT CCTCAAACAG GGGTTTGCTC 1360
|
| |
|
|
|