| Tag | Content |
|---|
EnhancerAtlas ID | HS073-14578 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:102195460-102196940 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr9:102195516-102195526 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr9:102195516-102195526 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr9:102195516-102195526 | AATGGAAAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 102195698 | 102196356 | | chr9 | 102195550 | 102196726 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I099432 | chr9 | 102195226 | 102197065 |
|
Enhancer Sequence | CCTTCAGTGC TTTAGGAATA TATTGCCTAG CATGAAATAT TCTTCTCTCT TGCCTGAATG 60
GAAAATTCTT TGTTCTTTCA AGACCCGGTT CAAATATCAC TTCCTCTCTG TGTTATTAAC 120
CTACGCTTGA TCTGCACTCC CCACAAATTA TTGTCAATGT CTAACATCAT GGCTGTGTAC 180
ATATCCTCTC TTCCACAAAA CAATGTACTC TTTTTATTTT ATAGTTTGGG AAACTCTGGC 240
CCCCAAACAC TAAGACTAAG TGACGTACTG AAGTTCAAGT TCACTCAGTT TGTCAACAGC 300
AGATCCAGGA CTACAAGATA ACCTAGGAAC AGAGCTCATC CCCATGGCCC CCCTATGATA 360
AAATGTCCCC TGCTTTTTTA GCCATAGCAA GTATCTGCTG GGCTGAGGCC TTGGTTGTCT 420
TTGAGAGTGA GGCTGTACCC CTCAAGGATG TGTCCTGTGT TGAGGGTAGC AGGGCCTGCC 480
TGCAAATATC CGGGTCAGCA GGCCAGGAGA GTTCACACTG AGGGGCTGGG CAGGGGTGTT 540
CAGGCTTTGC TCACAGGATG ACTCACGGAG AGGAAGTGCC ACTCAGATTT GTGAGTCACC 600
CTCTTGGGCT CCACAGAGGC CCTGTCACGC AGGAGCCTGT CAGCTTTCAT CTCCATCTCT 660
CCAACCCCTA GGGCCAAAAG TCAAACTTGG TTTCTGCTTA CTTGTTTGAT TTTTAGTGGC 720
TCCTCCAGCT CCAGAACCTT TAGCAAGCAG CTTCCTTTGA AAGTTTAAGA TGGAAATCTC 780
TAAGCTGGCC CTGTGCTTCC CCTGACAAGT GTGTAATCGA TGGGAAATCT CTCACTGGAG 840
GCTATCCTAT CTGGAGTCTT GATAAAAGGC ACTTTCAGAG AGGTGAAAGG CTCTTAGAGA 900
CCTTTTACAA AGAACTAAGC TGGCCTAAAA TTGTCACCTT TATCCTCCCA GGTGACCATT 960
CACTATCACC AACTCTCTGG CAGAGAAAAA TGTGAGGATA CAAACACAAA GAAAATCACT 1020
CCCTTAATAC ACACGGGGTA GAATCCTCTT TGGGTCAGAC AGAAAAGCAG TGACTTGGGA 1080
GAAAATTGTG AAGGGTGGTT GGATGCTAGG AGCTGACTGG GCTGCATCTT TGAGCTTTAG 1140
TTCTACCCTT CCAAGTCTCC TGTCCTCCTT GAAGTTCTCT GCTTTTGATT TCTGTGGCCA 1200
CCAGCACATA TGGCCCTGTT TCTCTTGAAC ATACTTGAAA TGGGCCAATA CTTTCTAAAA 1260
GGCTTTACTA ACACACTGAA GAAATGAACA TAGAGAAATA CCAATGGCAT TGAGAACAAT 1320
CCAGTTTACT CACAACTATA TCTTGGGCCT AAGAATCCCA GAGCAAGCAT AGGAGACCTT 1380
CATCAAGCTT TCCCAAAGCC CCTATTCAAT TCCACCCTCT GCCTTGCTTC TTCTCCAACA 1440
TTCCTGCCCT TCCCTCAGCC ATAAGGCTTC TGGGTACCAT 1480
|
