| Tag | Content |
|---|
EnhancerAtlas ID | HS059-47662 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr9:102195240-102196680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr9:102195255-102195266 | TTAATTAAATC | - | 6.02 | | 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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I099432 | chr9 | 102195226 | 102197065 |
|
Enhancer Sequence | CTTTGGGTGT TTTATTTAAT TAAATCATCA GGTGCCCAGT CACCCAACCC AGGAGCCAGC 60
AGGCCATCCT CTGTAGAATG CGGGAAGTGC GTTCCTACAG TGGACATCAC CTACTGATCC 120
TGCATCTAAA ACACCTCTAT GCTTCTCTCC CTCTCTCATG CTCTTGAATC CACTGCTCCT 180
CCCACATACT GGCTTCGTTA TCTCTCCCCT GCCTCTTCTG CCTTCAGTGC TTTAGGAATA 240
TATTGCCTAG CATGAAATAT TCTTCTCTCT TGCCTGAATG GAAAATTCTT TGTTCTTTCA 300
AGACCCGGTT CAAATATCAC TTCCTCTCTG TGTTATTAAC CTACGCTTGA TCTGCACTCC 360
CCACAAATTA TTGTCAATGT CTAACATCAT GGCTGTGTAC ATATCCTCTC TTCCACAAAA 420
CAATGTACTC TTTTTATTTT ATAGTTTGGG AAACTCTGGC CCCCAAACAC TAAGACTAAG 480
TGACGTACTG AAGTTCAAGT TCACTCAGTT TGTCAACAGC AGATCCAGGA CTACAAGATA 540
ACCTAGGAAC AGAGCTCATC CCCATGGCCC CCCTATGATA AAATGTCCCC TGCTTTTTTA 600
GCCATAGCAA GTATCTGCTG GGCTGAGGCC TTGGTTGTCT TTGAGAGTGA GGCTGTACCC 660
CTCAAGGATG TGTCCTGTGT TGAGGGTAGC AGGGCCTGCC TGCAAATATC CGGGTCAGCA 720
GGCCAGGAGA GTTCACACTG AGGGGCTGGG CAGGGGTGTT CAGGCTTTGC TCACAGGATG 780
ACTCACGGAG AGGAAGTGCC ACTCAGATTT GTGAGTCACC CTCTTGGGCT CCACAGAGGC 840
CCTGTCACGC AGGAGCCTGT CAGCTTTCAT CTCCATCTCT CCAACCCCTA GGGCCAAAAG 900
TCAAACTTGG TTTCTGCTTA CTTGTTTGAT TTTTAGTGGC TCCTCCAGCT CCAGAACCTT 960
TAGCAAGCAG CTTCCTTTGA AAGTTTAAGA TGGAAATCTC TAAGCTGGCC CTGTGCTTCC 1020
CCTGACAAGT GTGTAATCGA TGGGAAATCT CTCACTGGAG GCTATCCTAT CTGGAGTCTT 1080
GATAAAAGGC ACTTTCAGAG AGGTGAAAGG CTCTTAGAGA CCTTTTACAA AGAACTAAGC 1140
TGGCCTAAAA TTGTCACCTT TATCCTCCCA GGTGACCATT CACTATCACC AACTCTCTGG 1200
CAGAGAAAAA TGTGAGGATA CAAACACAAA GAAAATCACT CCCTTAATAC ACACGGGGTA 1260
GAATCCTCTT TGGGTCAGAC AGAAAAGCAG TGACTTGGGA GAAAATTGTG AAGGGTGGTT 1320
GGATGCTAGG AGCTGACTGG GCTGCATCTT TGAGCTTTAG TTCTACCCTT CCAAGTCTCC 1380
TGTCCTCCTT GAAGTTCTCT GCTTTTGATT TCTGTGGCCA CCAGCACATA TGGCCCTGTT 1440
|
