Tag | Content |
---|
EnhancerAtlas ID | HS059-03417 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr1:180820570-180822250 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr1:180820682-180820692 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:180820682-180820692 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:180820682-180820692 | ATTTTCCATT | + | 6.02 | RUNX1 | MA0002.2 | chr1:180821333-180821344 | TTCTGTGGTTT | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTATTGGCAT TTATCCACAA TTTATACAGA ATTATAAAAT AACTCCAAGA CCAGAAAAGG 60 CACAAACTCC ATAGAAACAT AACCTAGAAA GGTATGGTGT AAACAATGCA TAATTTTCCA 120 TTTTAGTGCA TAGTAATTAT TTTTGCTTAT TCCAAAGTCT TAACTTTTCC TTACAGCAAT 180 AACCTACTAC AAGAATGTTT CCAAGGCTGT TGATCAAATG TGTAACAGAA AGGGATTTTT 240 AAAAATAAGC CTAGACACAC ATACATAAGA AAGATATTGG AAGAGGTTCT GATGATCTGA 300 TCTGGGAAGG GGTATCTGAT ACAGCAGAAG AAAAGTTGCT AAACTCTGTC AAGAAAGGAA 360 GTCCTAAATG GTGTCATTGA TGCTTTTATA ATCACTGAAG AGGTAACTTT GTTATTGAGG 420 AGCCAGTAAA TAAGGATCTA TATGGATAAT AAATTGAATA TAAATAGTTT AATAATGAAA 480 TTACTTTCTT GATTACATCA GTCACATCCA GTTTTATTCA ACAAACATTT ACAAAACATC 540 TTCAATGTAT CAGGCACTAC TAGATGCTAG GCATACATAG ATGAACAAAA CATATCTTGC 600 CTTTAAAACC TCCTCTTGGA GCTCACGGTT TGGTAAGGGA AATAGACTAA TTACAATAGA 660 ACATGGAAGT GCAATAATAC TATATTATCA GTATTGTATA GGGTATAAGG TGGTTTCAAA 720 GAGGAAGTGG TTAACTCAGT GAAGGTTTTG AGGAACAGTC AAGTTCTGTG GTTTTTTTTT 780 AATTAAACAT TTTGTTTTGA GATAATTGTA GAATCACATG CATGGCAAGA AGTAATGCAG 840 AGAGATCCCA TATACCCTTT GCATAGTTTC CCCAGTGGTA ACACTTTACA AACATAGTAT 900 AATATCACAG CCAGAATATT GACATTCATA CAGTCAAGAT ACAGAACATT TCCATCACCA 960 CAAGGATCCC CCCTGTTGCC TTTTTTGCAC AGTATTCCCC CGACCCTATC CATACCTTCA 1020 CTTTCTGCAG TTTTACTTAT CGGTGGTCAA CCACAGTCTG AAAACTTTAT GCTATTTTGA 1080 GAGAGAAAGA GACCACAGTC ACATAACTCT TATGGTTTTC GTTTTGTTTT TTGAGACAGG 1140 GTCTCACTCT GTCACCCAGG CAGGAGTGCA ATGGTGTAAT CTCAGCTCAC TGCAGCCTTG 1200 ACCTCTTGGG CTCATGCAGC CCTCTCACCT CAGCCTCCTG AGTAGCTAGG ACTACAGGTG 1260 TGCGCCACCA CACTGGTTTA ATTTTGTTTA TTTTTTGTAA AGGTGAGGTC TCCAACTCCT 1320 GGACTGAAGC AATCCTCTCA CTTCGGCCTC CCAAAATGTT GGGATTACAG GCGTGAGCCA 1380 CCACGTCCAG CCTTCCACAT AACTTATTAC AGTATATTAT GATTGTTCTG CTTTATTATT 1440 ATTGCTAGTC TCTTGCTGTG CTTAATTTAT AGATTAAACT TTATCATAGC AGTACTATCC 1500 ATGGTTTCAG GCACCAACTG GGGGTTTTGG AATGTATCCC CCACAGATTG CAATGGTGCA 1560 ATCTCAGCTT ACTGCAGCCT CCACCCGTTG GGTTCAAGCA CTTCTCATGC CTCAGCCTCC 1620 CAAGTAGCTG GAATTACAGG CGCACACCAA GCCCAGTTAA TTTTTGTATT TTTAGGAGAG 1680
|
| |
|
|
|