| Tag | Content |
|---|
EnhancerAtlas ID | HS146-02172 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr10:100103480-100105200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr10:100104854-100104866 | TCCTGTTTACTT | - | 6.07 | | Foxo1 | MA0480.1 | chr10:100104854-100104865 | TCCTGTTTACT | + | 6.32 | | Nkx3-2 | MA0122.3 | chr10:100105184-100105197 | ATTAAGTGGTTTT | - | 7.22 | | TBXT | MA0009.2 | chr10:100104602-100104618 | TCACATAAATGTGTGA | + | 6.08 | | TBXT | MA0009.2 | chr10:100104602-100104618 | TCACATAAATGTGTGA | - | 6.16 | | ZNF143 | MA0088.2 | chr10:100103619-100103635 | GAGTGCATGGTGGGAA | - | 6.06 |
|
| | 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 |
| GH10I098344 | chr10 | 100104143 | 100105092 |
|
Enhancer Sequence | CACAGCTTCG CTGGCTTGGA TCCCTAGTTT ACATTTTTAC TTTGCTTTTG ACTCCCTGGT 60
TTTCATTTTA CTTCCACCCC ACATGTCATT TTAAGGACAA CTCATGCTGC TCACTATAGA 120
CCAATATGGT CTAACTATTG AGTGCATGGT GGGAATGCTC ATTCAGTTGG CCCCAGGCCC 180
TAATAATAAT AATAATTACC ACAGCTCAGA GCCTTGAATC TGCTACTGGG ACCAGGCTAC 240
TTGGAAAAGA TGACCTTCTG CAGGGTCCAG ATCCAGCTGG TGAAGGTGGG AGGGAAGAAG 300
ATGAAAAGCC TCTGCTCCCC TCTGTCATGC CGCTTCATCT TACCTTCCCT TGCAAAGTTA 360
AAGTCTGCTT CGAGTCTATT TGGTTCCTTG TAGAGAGCCT GCTTCCCACT ATGCCTCTGT 420
CTTACCTGGT GTCTTTGGCA GAGCCCCGAA CCATCTCAGT GTCAAATCCC GGGGCTCCCC 480
TATTTGGCCC TGGTCTAGGT AACTGAACAG TCCCTGCAAA CACGAGGGAT TGATGTATGT 540
CCAATGCAGG TATGTCATGA AAAGGTTCCA CAGCAGAGTG ACTAAGGAAC CAATTAGGAG 600
ATGAATAAAA CATGTCCTAT GTAGGTTATT CAAGAAAAGA CTAATAATGA GAAATCCGAA 660
GAAAGACGGG TGCATTCATT TTGGGATCGT CCCTTCTTGA GCAAGTAGAA GGAAGGCCTG 720
AGAGTCAGTC CTTCAAGGGC ACAGCAGCCA GGGGAGGTGC TGAGTGATGG AGGCAGAAAC 780
ATTTTTTGCC CCTCATTTAG CTGACTTCCA AACACTGCCT CCTCCTCCTC CTCTGTGGTT 840
GGGAGATTTC ACATTTTGCT TGTCCCAAAG CCCCAGGACC CGCTGACCCA GCATGGTTGT 900
TTCCTTCAGC TGTTGCTATG ACCTGACCCC AAATCCTGGC TATTGACTGA GTGGCCACTT 960
GACTTCGCCA GATGTCTCAC TCTGCACTTC CTGATGTGGA AATCTACCCC CTATCCAGAG 1020
TAGGGCCTCT GGATGCTGGC CAGCCTCTTC CTGGCTCCCT GCATCAACGT CCTCCCTACA 1080
AAGGCTGAGA TGCAAGATCT GTTTTCCAAA CCACCAAAGT CATCACATAA ATGTGTGAAT 1140
GCATACATTT GCCAAAAAAC CGGCAGATAA TACTACTAAT GACTAAACCA GAGCTGGCTT 1200
GGGAAATGAG GGTAAGTCAT CAGCAAACTC GTCAATGAGT GGCAGTGAGG CGCTGTAGAG 1260
AGCAGCTGGT GTCAGAGGCT ATGAGTTCCT GCACCCTCAC TGGCTGCATT GCTACTAAAA 1320
TAAGTCTCAG TTTCCTCATT TGCAAAGTGG GCTTAATAAT CAGAATAATG CTTATCCTGT 1380
TTACTTTACA AGGTTCTTGC TAGGATCAGA GCCCTATGAA CTTTTTTTTT TTAGAAAGCT 1440
ATACTTGCAT ACAAGACTAT TCGTTTCATA ATTAGCAAAG TGCCTTGCTG AAAATAAGTG 1500
CTCACTAGGC ATTAGAACTG TAGTCTGATT GTGAAAGAAA ACATTATTAT TTCATGGCAT 1560
TTCCTACCTG ACTTTCTTCT TTGTTTGCCC GTCTTCCCTG CCTCCCCCAT TAGACTGTAA 1620
ACCCTCTGAA ATCAGGAACT CTGTCCATCT TGCTCAGAGC TATGTTCCTT GTGCCTTGAG 1680
GGGTACTGGA ACAAAGAAAA TGTCATTAAG TGGTTTTTGA 1720
|
