| Tag | Content |
|---|
EnhancerAtlas ID | HS098-07968 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr10:95706380-95707860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr10:95707551-95707562 | AACCAATCAGA | + | 6.62 |
| | | 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 |
| GH10I093945 | chr10 | 95705348 | 95708145 |
| Enhancer Sequence | TAAATCTTAG AAAACAGCAG GAACTAAGGG GTTCAGAGAC CCTTAATAGA AACAAGCATT 60
ACCCTTCAAG ATAAGTAGGT TTGATGATTT TCAGCCATTT TAAAACTTTT CGTGCTCTAC 120
TCCACTCAAA TTTCAGAGAG TGAATATTGG AATGATTTAG TTTGGGACTT CTGCCCATGC 180
CGTGGTCAAG GGAGGGACAC TTGACATGTA TGCTGAATCT ATGTTATTTC TGACTGGAGG 240
TGAGTATTGG TTTTCTTAAG CGAAAGCTGG GTGTTGTTAT CAGGAGAAGG GAGTGGAGAG 300
GCCAAGCGGG CAAAACAACA GATGTCCATG AACCTGGTGC CAGGAATGTG GCCTCTCCAT 360
CCCCTTGGAG GGATCTATGA CATGGGTTTG AGGCTAGGGG CAGATATAAA CCATGAATAG 420
AAATAAAGAT AAATGCTGGA TCAAAGCTGT GGCCCAGGTC AGGAAGGGGC AGGCCTGAGC 480
CAGGAGAGAT GGATGACAGA GAGGGCACTT GGAGTTCTGA GGTGTGAGCA GCTGTATTTT 540
CTGATACGCA CTTCATCTAG CCGCCTGCAC CGAGAATGTA CCACATGGTC AGTAGAATGG 600
AATGTAGGGC AGACACCAGC CCCTCGGAAG CACACAGAAA CCTGATATAG TGGCTTCAGC 660
CGGATGCCTA ATTCCCTGTG GTGTCCAACG AACGGAAATA TGAGGCTGGC CAGGCCATGT 720
GAGAGAGTAA GACCAGCCAA GTGAGAGTTA TCAGGGCCGA ACTGCACATT TAGGTGAGAC 780
CAGGGAGGTT AGCTGAGGCA CAGAGAAACT GCCCCATTCT CTTTCTTAAG CGGAGGCTTA 840
CCCGGCTAGC AACAGAGAGG GGTCCTCGTT GAGGCAGAAA GTGCTGGCAC CAGAGAGGGT 900
AGAGGAAACT CCTGTGATAG ATGCATGAAG TGCAGTCTCA TTTGGAGCCA ACAGCTGGGG 960
CAAAGCAGCA ATATGAATTA CCAGATATAA GAGGTCAGTT TGAGACTGTG GTAAAGAATG 1020
AGGCAAGAGA CCAGAAGCTT TGATAAGAAA CAGGTCTAGA AACACAGTGG GAAGTAGGAT 1080
GGCTTGAGAA AGTTCAGTAT ACAAACTGAA CTGCCCAAGA AACCAAAGCC TTGTTCTCAT 1140
TGGGTGCTGG TCACATGACA GGGGGCTAGG CAACCAATCA GACCACTTAA TAGTATAGAG 1200
CTGGGTTGGA AAAAAATAGG CAAATACTCT AGGTCTACCT GGGCACCTTG TCCAGAGAGG 1260
ACATCCACTG AAGTGAACTG CAGGCAGGAA ACAGAGGTCT GAAGGGGAGA AGCCAGGGTC 1320
CTACAGTCAG AGAGCCAGCC AGGTGGGCAC TAATCAGTAC GATAGATCCC TGCTCCCAAT 1380
GCAGATATCC ATCGAGGGAG GACACCAGGT TGCTGGTCTT GGTAATGTTT ATTAAGTGTG 1440
AGCCTCTGTC TAATTGGGCA AGTGTCAATT CTTAATCCAG 1480
|
| |
|
|
|
