Tag | Content |
---|
EnhancerAtlas ID | HS052-26599 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr3:99128750-99130240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr3:99129411-99129421 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr3:99129411-99129421 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr3:99129411-99129421 | AATGGAAAAT | - | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 99128850 | 99129136 | chr3 | 99129544 | 99130174 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I099409 | chr3 | 99128797 | 99131021 |
|
Enhancer Sequence | TCTCCAGTAG CCTCCTACTG CATTTAGAAC AAAATTCACT CTTTTTCATG GTCCATTAGG 60 TTCTACATGA TTGACCCTAT TCTTATCTAT GACTTCTCCC AGCTTTACCC CATCTCTCTA 120 TGCTCTTGCC ACATTGCCCT TCTAGAGTAG GTTAAGATAT TTCCTTTCTT GAGGCCTTTG 180 CTCCTGTTGA TCCCTCATGC TGGAATTCTC TTCCTCCAGG CCTTTGCATA GCTGGTTCCT 240 CTAGTCACTA AGCCTTAGCT CAGAGGTCAC CTCCTCACTG ACATTCACTT ATAAGTAGCC 300 CTTCCTCACT GGCCTCCCCA ACACTTTCTA TTACAACACT CTGTCTTATT TCATAGCATG 360 CACCACTAAT CTTATTTATT CAGTTATTTG ATTATCGCTG CCTCCTTATC CCAATGCCAT 420 CCCTTGAGAG GGGATCTAGT CTGCATGGTT TAGTCCTCTA TGCCTTCAGT AGTGTCTGGC 480 ATACAGTCAG CTCTCATTTA ATATTTGTTA AATGAGCAAA CAAAGTCTCT CTCGTATAAG 540 TCAATATAAT TCTAGCTATG AGAAATTCCT GTTCTGTGCT AGTCTTGAGG ATGTGAAAAT 600 ATGAGGGGAA ATTAACATTT TTCAGCAAGC ACTGCTAGAG ATCCAGGAGT TTCCCCCTCA 660 CAATGGAAAA TTTAAACCAT GAAGGAAAAT AAATGAAGGT TAAATACTAG AAGATATTTG 720 TGGACAGTTA TGCATTCATT CCACAGGCTC TGTAAGCCTG TAAACAATCA GGAGTTTATA 780 CCACATCTTA GCTGGTGTTC CGCTGCTTTC TATAGAATGG GAAGAAAATG TAGCTTGTCT 840 ATCACAGCAG GACTGGTGGC TTGAAAGGCA GCAGGATTTG TGTTTTCAGG TGTGACAGAC 900 TCTCTCACCC TCAGCTCCCA GAGGGCAGAG ACCAAGGACC ACATAACCAC CAAAGCCAAT 960 GATCTGACCT CTGGAGGATT GACAGGCTCC AGGATGAGTA ATGAGTTAGG CCCGGCAGAT 1020 TATACAGTGC CCCTGAGATG AAGAAAACAG AACAAGGATG AATGAGTGCC TGTGGGAAAA 1080 GAAGTGTATC GGCTCTCACA CAACCACCGT GCCCTGCGTG ACTGGCTTAA ACAGAAATCT 1140 GGCAGCAAGA GAGGGAACTA AAGGAAGTTA AAAAAAAATA GCAGGCAATC TCCTCCCTTT 1200 TCATTCTTTA ACTTTCTGAT GAGAGAATAA AATGCTGCTA CCAGATGTAG CATGTGCTGG 1260 CATTAATTAT CTCATTCTTC CATCATCAAG AAAGAATCAA TTCATATCAT CGTTAGCGTG 1320 AGACCACTTC AGAGAAAGCA GGATGTTGCT GTAATTAATC GTTCAAGCTC TGGATTCCAC 1380 ACAGACCTGG ACTCAAATTA TGGTTGTTAT CATTTAGGGC CATGACACCT TTTACAACAG 1440 GAACATTTTA CTACCACTAC ATGAGGTTAT GTAAGGAAAA CATAGACAGT 1490
|