| Tag | Content |
|---|
EnhancerAtlas ID | HS145-18932 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:197121330-197122410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr3:197121579-197121590 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chr3:197121579-197121590 | GATGAGTCACC | - | 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 |
| GH03I197392 | chr3 | 197119359 | 197123101 |
|
Enhancer Sequence | ATGAGAACGG CATGGAGAAG GGGGAGGCGC AAGCAGCTGG AAGCCCACGG CGGAATGGGC 60
CGGTGCTCGG AGAGCTGTTC GGATGGCACG GGAGCTGATT GTCTTGACGT TAAGTTCCTC 120
GGTGAGGAGA GAACAGAAGT TAATGGCACC CACCGGGCCT GGGTGGAGCC TCAGCACCAC 180
CAAAGAAAGC AGATTCTGCA TTTGGAAAGC CTAGGCCCTC TCCTTGAACC TGGTTCTCAA 240
GGTTTCGGTG ATGAGTCACC TCGTTCCCCC TCACCAGCTT CTGTCTTTAG CCACAGCACT 300
GACGTGTCTG AACCCGCACG CACCTCCTGA GCTGGAGCAC CCGTCATCTT CACACCACAG 360
ATGACTAACC ATGGCCTGCT CACAGTCTCC TCATTATCAC GGAATGAAAA TGCTACATGC 420
CTGAAAGCTG AGGTTTTGGG AACAGGATGA GAAGAGCTGC GGAAGGAATG GAGATGCAGG 480
TGGCAATGAG CTAAGCTTTT GACAGGCCCT CGCAGTCCTC GGGAGCAGGG GCCAAGTGAC 540
CACAGATCCA GAGAGAGTGC TCTCCTTGGC AGGGCCGCAT GAAATCTCAT TCATTACAGC 600
CTCCGATTAG GTTCCCAGGC TCATTAAAAT CTGTGTGCCA TTCACTGTTT CTCTTGGATC 660
AGACTGGATT CTACTGTGCA GAGAATTGCC AGGGCTTCCA AGTGTCCAGT GCAGGCCAGA 720
TAGCATCTCT TGGCTTCACT TCTTCCTGAA GTTTCTCCCT GTGCTTCTGT GTGCTCACTG 780
CCAAGAACAC AAGTCAGCAT TCAGGCCCAC GGCTGCCAGC TGAAACAAGG GCTTCTGACC 840
CAGACAAAGC CCGCAGATAA AGTCCAAAGC ACTTGAGCTA AACTTACTCT AAAAACTATG 900
GCAGTACAGG ACAAAGGAAG ACACTCGGGT TAGACACAAA GAACCACAGC TAAGGCAACC 960
TTTAAAAAAG GAGAGTGGGC TGGGCGCAGT GGCTCATGCC TGTAATCCCA GCACTTTGGG 1020
AGGCCAAGGT GGGCGGATCA CTTGAGCTCA GGAGTTCGAG ACCAGCTTGG GCAACATGGC 1080
|
