| Tag | Content |
|---|
EnhancerAtlas ID | HS177-09319 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr17:47337200-47338600 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr17:47338191-47338202 | CATGAGTCACC | - | 6.62 | | FOSL2 | MA0478.1 | chr17:47338192-47338203 | ATGAGTCACCC | - | 6.14 | | JUNB | MA0490.1 | chr17:47338192-47338203 | ATGAGTCACCC | - | 6.32 | | JUND | MA0491.1 | chr17:47338191-47338202 | CATGAGTCACC | - | 6.02 |
|
| | 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 |
| GH17I049259 | chr17 | 47336904 | 47338798 |
|
Enhancer Sequence | GGTCTCCCTC CCCCGTGGTC TGGAGATCCT TGACATCTGC CATCCCCTTA GCAGAAGCTG 60
CAGCCAGAGA AAGAGGGCGA CGGTCCCGTC ACATTCTGAG CCCAGCAACG GAGGGCTTTC 120
CAGGCCGGGA CTGCGGGCAG ATGGGAATTC TCCTCTCCTT TCTGCTGGAC GTATCTCCCC 180
TCAGTTTCGC TATCTGTAAG ATGGGGCATT GTCCCTGCCA AACCCGCAGG CCAGGACGGC 240
CTAAGAGGAT CAAACGAGGA GAGGCAACGA GGATTGGTGC CTGGCTTTTC CTGAAAACAG 300
ATTCCTCCCC CGCCCCCGGG ACCTGTCCCA CAGGGGCGTC TGGAAATTCC ACAGAGCCAG 360
CCAGTCTCAG AGTGAAACAA TCGGATCCGC CGCGACACAG CAGCTATTCA GACGTCGGGG 420
GCGGGGGCCG GGCCGCTGAG CGAGCAGAGC AATGCCGCCC TCGCGTCCCC TCCCGGCCCA 480
CGCGGCTGCC CCGGCCGCCC TCCCCGCGGA GCCCCGGCCT CGCACGGGCC TCGGCGCCCG 540
CCGGGCGTCC CCCAAGCTTC CTTGTTTGTG GCCGAGCGAC CGCGGAGCGT GGCACGTTCA 600
GGAAGGACGA GTCGCCCCAC GGCGGGGAAC CGGCGACCGG CGGCAGCCCC AGCCCAACCC 660
CGGCCACGCC TCGTTAGGCG CCACGTCCCG TCCCCGGGCG CCCGGAGCAC TGTGCCCCGC 720
CGGCCCCTGC CCGCCGCTCG CTGTAGGAGG GAGCCTTCTG CGTCGGCTCC CGACACTCGC 780
TCACTGGGGC GCGGGCACTT GAGAGTAGGC AACCTGGGGG CCCCAGAAGG GGATGGGGCT 840
CCGACAGCTT CAGCCGGGCG TCCCCTCAGC TGCCTTAGCT GGCGTCTGAG AGCGACTCCT 900
CCGTCCAGGG CTGACAGTTC CCTTGCCCCT TAAGAGCCAA TCGGAGAATC ATAGGATCTG 960
ACATCCTGTG GCTCAGCCGG GTCTAAGAGC TCATGAGTCA CCCTGTGTGC TTTGCTGATG 1020
AGGAAACCGA GGCCCAGAGA CGGGGGCTGA CTTATTCGAG CCACGTTTGT GTCTCCTAGC 1080
CCTGTGCCCT TTCTCCAACA CTCTACTATC CTACCTCAAA TCAAATCCAC TCTGGGGCTA 1140
AGGACATCTA GAAGTGTGCG TGTGTGTGTG TGTGTGTGTG TGCGCGCGCG CCAAGAGTGG 1200
CTTGGCTACA TTAGGGAAAT GCCAGAAAAA TGGAAGGTTT CTAATAAAAG CTGCTCTCCA 1260
CGGGCCCAGA GTGTGGGGCT CCCACCCATT GGCTCCACAA ATCACCTGTA CAACCTTGCC 1320
AGACATTGGC CGCCTGGCAG CTCCAGACTT CACTCCACCC ACACTCCCCA CACACATACA 1380
GACAATGGCA TTTTTTTCTA 1400
|
