| Tag | Content |
|---|
EnhancerAtlas ID | HS095-31096 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr9:87350430-87352650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr9:87352135-87352145 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr9:87352135-87352145 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr9:87352135-87352145 | AATGGAAAAT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTTCCCTGA GGATATCAAA TAGTAATAAC AATACAAATA TAGAATAGAT GGTGCACAGA 60
GATGCCCTTT AATTGGTTTT GGCATAAAGT TGGATGAATT CAATATGTGG CTTAAGAAGG 120
CTAGGGAGAG TGAACAAAAA GTAGAGACAG CAGTTGCAGG CACGTACACA CACACAGGGT 180
GGGGTTATCT GAGGAATCTT CAAAAGTTCT CATGTATCCT ATTTAGCTTA CCAGCCAAAA 240
AGAAAGACTT GTCTAAGATG AAATTGATCC ACTGTATGTC AGTCATTGAA ATTCAATCCT 300
CCATATAAAA ATCCCTTCAT GAACCAGAAA GTGTACATGG AGACTGAGTG GAGATTAGAA 360
GTGATGAAGG TTTCTTTTTG AGTAGAATTT GAGGCAGAAA TTAATGGCAG AGAGATCACT 420
TATGATTTGT TGTGAGGAAG AAACCTGAAG CCTTTGTTAG CATTTTCTGA TCAGATAGCC 480
CAAGTTGCAA CAATTTTGAA GGCCAGGTAG TCCTATAAAT GTGAACATCA CGTTGATGCA 540
AAGTAGATTC TGTTCAGAAT CATTACCCAA GTGATTTAAC CCTTTGGCTT GGAACAAACC 600
TAACCAGAGC ACCAGATGAT AAAATACCCT CGTTTTAAAG CTTACCATTC TTTAGGCAGT 660
ACATAAAGAG TGTCTGTATG GCCCACTCAT TCAGGAAGAA TGTCACAGCT CAAGAATGCT 720
CATTCACACA AGCAGTGGGA GTCAGTGACT TGCGCTTCCT AATTCGGGAG CTCCTGTCTC 780
CTATGCGAAA TGCGCGTCAG GAACAAACTA TAAATATTGG AAGAGCTTTT CCCACAGCTT 840
CTCCTTCCGT GCTGTTTTAT CGAAAGATTC ATGACATCTG GATGAACTAG AGCTCTCTGC 900
GGCACTTAGA ATGCCCCACA CTGGTGGATT TAGATTTGGT GTACTTAGTC TAAAGAACGA 960
GGGGAGAGGA AATTTCTCCA AATGTTATGC ATTAAATAAA GCTCTCCTGG CTTTATACTA 1020
TTTGTTCCTT TGGTCTTTTG TCAGGACCTA TTTCTTGTCC TGGAGGTGAA GGAGAGAAAT 1080
TTATGTCTGC TTTTCTGCCT TAAATAACTG AGAAGAGAAT GATTTGGCCA TACATTCAGA 1140
ATAATGATAA TTAAGATTTA TACTTAAATA GCTTCTTATA CCTCAGGAGT GCTAATGTTA 1200
GTTAATTATG CTTCCCAAAG CTCCTGAGGA ATTGCCAGAG CCAATGCTAT TATCCTCTCC 1260
TGTCTTATAG AAGACTCCAT TGTTACAGAA AAAGTGGAGA CTCCCACTGC TATATAGCAA 1320
ATGAGTGGTT CAGCCAGAAA GGAAACCAGA TATTGCAATG CCAATTTCAG GCGCTGAGTT 1380
CAGCCTGCCC TTCTGAAAGA GAAGAGAAGA ACCTGAAAAT CAAAAGGCTG ATCCCCCCAT 1440
GAGTGAGAAA ATACTGTCGG CAAAGCAAGG ACAGTTTATT TGAATAGAAC AAATCTTTTG 1500
TAATTGCCTT ATCATATGGA ATTCTTTGAA ATATTTTTCA GGATCACATG ATCACATTAA 1560
ATAGAGTCTG CAAATAGAAT GGATAGAAAA GTCTTTTCTC TCTCTCTTTT TCTTTAGGTA 1620
GAGCATTAGA GGGAGACTAA AAGTTTAAAG GAAGGAAACA GATGTGTCTT CCTGGCCTCC 1680
CCATTATTTT TTATCTTGTT AGCAGAATGG AAAATGAACC CTACTGTCAG GCTACCTCTC 1740
TTCCCACAAT ATATTTTTTT TTATCCAACA AACCTGTTTT TCCTTTAACT ATAGAGTCTT 1800
AACAGTTGAA ATGTCATAAA GATGTTTTCT CTTTCATCAA GATTTACATA AAGTCATAAG 1860
ATTATTCATG AGCTATAAGT GAGTTTAGAA GATGGAAATA AAAAGGTCCT ATTTTAGGTT 1920
ATTTTGCATG GAATTAGGAG GATGGTGCAG TGCTTGGGTT TGATGCTGTT GGGGAAAGAG 1980
GAAAGTGATT CCATCTTTGA TGTGTGGAAG ACCAAATGCC CTCAGGGCTC ATCTGCCTCT 2040
TGGAGGTGCA GACCTCACTG GCTCCCTGGG AAGCTTTGTC AGGAGTGCGG CTGTGGCTGT 2100
GATACAGTTG CTATCCTTCT TTTACTATTT TTTTCAACTT GTATTTTAGA ATCGGGGTGC 2160
ATGTACAGGT TTGTTACGTG GGTCTATTAT GTGATGCTGA GGATGGGGAT GTGACTGAAC 2220
|
| |
|
|
|
