| Tag | Content |
|---|
EnhancerAtlas ID | HS081-14453 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr3:197121140-197122170 |
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 | AATCGCTTGA ACCTGGGCGG CGGAGCTTGC AGTGAGCTGA GGTTGCGCCA CTGCACTCCA 60
ACCTGGGCCA CAAGAGTGAA ACTCCGTCTC AAAGAAAAAA GGTCTATTTT TAAAAACTAC 120
TAACTGAGAA AGAAGTAAGA GCCTTGAAGA AACAGAAAGA AGGAACCTGA GCATGCCACG 180
GCAGGAGAGG ATGAGAACGG CATGGAGAAG GGGGAGGCGC AAGCAGCTGG AAGCCCACGG 240
CGGAATGGGC CGGTGCTCGG AGAGCTGTTC GGATGGCACG GGAGCTGATT GTCTTGACGT 300
TAAGTTCCTC GGTGAGGAGA GAACAGAAGT TAATGGCACC CACCGGGCCT GGGTGGAGCC 360
TCAGCACCAC CAAAGAAAGC AGATTCTGCA TTTGGAAAGC CTAGGCCCTC TCCTTGAACC 420
TGGTTCTCAA GGTTTCGGTG ATGAGTCACC TCGTTCCCCC TCACCAGCTT CTGTCTTTAG 480
CCACAGCACT GACGTGTCTG AACCCGCACG CACCTCCTGA GCTGGAGCAC CCGTCATCTT 540
CACACCACAG ATGACTAACC ATGGCCTGCT CACAGTCTCC TCATTATCAC GGAATGAAAA 600
TGCTACATGC CTGAAAGCTG AGGTTTTGGG AACAGGATGA GAAGAGCTGC GGAAGGAATG 660
GAGATGCAGG TGGCAATGAG CTAAGCTTTT GACAGGCCCT CGCAGTCCTC GGGAGCAGGG 720
GCCAAGTGAC CACAGATCCA GAGAGAGTGC TCTCCTTGGC AGGGCCGCAT GAAATCTCAT 780
TCATTACAGC CTCCGATTAG GTTCCCAGGC TCATTAAAAT CTGTGTGCCA TTCACTGTTT 840
CTCTTGGATC AGACTGGATT CTACTGTGCA GAGAATTGCC AGGGCTTCCA AGTGTCCAGT 900
GCAGGCCAGA TAGCATCTCT TGGCTTCACT TCTTCCTGAA GTTTCTCCCT GTGCTTCTGT 960
GTGCTCACTG CCAAGAACAC AAGTCAGCAT TCAGGCCCAC GGCTGCCAGC TGAAACAAGG 1020
GCTTCTGACC 1030
|
