| Tag | Content |
|---|
EnhancerAtlas ID | HS177-22777 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr8:80199560-80200850 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr8:80199846-80199857 | TATGACCTTGA | - | 6.62 | | Esrra | MA0592.2 | chr8:80199847-80199858 | ATGACCTTGAA | - | 6.62 | | Esrrg | MA0643.1 | chr8:80199847-80199857 | ATGACCTTGA | - | 6.02 | | LMX1B | MA0703.2 | chr8:80200246-80200257 | GTTTTAATTAA | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 80199600 | 80200000 | | chr8 | 80200332 | 80200584 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I079287 | chr8 | 80199519 | 80201870 |
|
Enhancer Sequence | GGAATTAACC AATCTTACTG TGTATTCCTA ACCTTTCATC TCTGTTCTGA TGGTGTGGTC 60
TGTTAGCCTG GGACCACCCT TCATCTCTGT CCTATGGGTC TCTTGCACCT GCAGCCTTAG 120
GCTCACCTAT ATCCTTGTTT CCATGACCTT ATAGTGACTC TCACTCAGAG CATTCTAGCA 180
ACAAAATAAT TATCTCTTTT CTTAGCTTCC TGTTTACCCT GTTCTTTATG AGAAGCCTGT 240
TTTTCAGCTA ACGGCCCCAA GGGGGCTAGA CTTCCCTCCC TTCAAATATG ACCTTGAAGG 300
TCTTGATGCA TGTTGAGAAG GGAAAGAGAG GCTACACGAA GAGGTGGGAG AAGGTGAGAG 360
GAATACTCAT GGAAAGCCTT CATATGCTCG CAAAAACAGC AGCCCTAGGA TTCGAGAGGA 420
GACTTATTTG CCCTCTTGAC ATAAACTACT AACCTCTGGA GGATTTGGGG CTTGGGGTAA 480
GAACTCACAA ATGGAAAACA AATAATTTCC CCTCATCCAA AAGGGGTGCT AACTCAAAAA 540
AGGCAAGTAG GTGGGATCCT TAGAAGGCCA GAGTGAGGTC TTACGCAGCT GGACAAACTG 600
CTTCAAAAGC CACCAGAAAA CTCGGCCCTA GGGCATAACA GGAATGAAAA GCATATGATA 660
AGTCATAAGG ATCTGGCAGA GCCGGAGTTT TAATTAATGT CTGTCCCAGC AATGTGCCAG 720
GAGACAGGGG GAGGGTTGCA GGTCATCCGA GCTGGTAGGG TAAGAACAAG TATAAATCTC 780
GGGGGATATC TGCAAGGGAG CCTGAGTCTT TGCTGTCACA CAATGCAATT AAGAGCTGCA 840
GGCTCATGAA TAACAGGGAG TGTGTGTTTT TAAGGCAGAG AAGGAAGTCA CGCAGCATGC 900
CATATGAAAC CAAAGAAAAG GCCGACTTGC CCTCTGAGTC AGACAGTCTG GCTGGTGCGC 960
AAGGCTATTT CAGAACACAC ACACAGAAAA CAGAATAGGC AGTGCAGGTT CTTGGGAAAG 1020
AGCCGATTTT AGTTGAAAAA TGCAGAGAAA ACCCCAGACA TTGCACGGTT TTAGGGTTTT 1080
AGGCTTTAGC CCTACCACCC TGGCAAGCCT CCTAAGAGGG CCATTAATGC CTCAGTACCA 1140
CTCGGTGCAG ACCCCACAGT CCTTCCAGAC CCCGCGAGCC CATTCAGGGT GAGCTGAAGA 1200
TCCGCCGAAG GAGCAGAGTC ACTTATCCCC GAGAAGAATT GTTCTGGGGG CTGGATAGTG 1260
AACAGGAGAG TGAAAGGGGA GAAGAAAGCC 1290
|
