| Tag | Content |
|---|
EnhancerAtlas ID | HS148-00776 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:95044990-95046400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:95045547-95045558 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr1:95045547-95045558 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr1:95045543-95045558 | ATGGCTGAGTCATCC | - | 6.36 | | YY1 | MA0095.2 | chr1:95046382-95046394 | TCAGCCATCTTG | - | 6.04 |
|
| | 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 |
| GH01I094579 | chr1 | 95044561 | 95046719 |
|
Enhancer Sequence | TTTTTCCCTA ACCTGGAGGT ATCACCGGTG AAGGCTGTGA AAAAGCAAAG ATGGCAGCCT 60
GCCCCTTCCT CTGGAAGGTC CTCCATCCCA GAGGGTACTG ACCTGTTGCC AGCCTGAATG 120
TGCCTGTAGG AAGTGGCTAG AGATCCCGGT CTTTCAGTCA GGAGGAATGG GATCAGAGAT 180
CTGCTTAAAG AAGCAGTTTG GCTGCTTTTT TGTAGAGCAG CTGTGCTGTG TTGGGGATCC 240
CTTCAGCCCC CAGTTGGTTT AGGTTCTGCA ATATCCTCAG GCTGGACCAG CTGAGATGCC 300
CAAACAGCCA AGGTGTTGGC CTGCCCCACC ACCCCAGGCT CCCCATCCCA GGGAGAAATT 360
AGAACTCTGT CGGCCATAGA ACATGGGCAG GGAAGGCCAA GTCCTCTGCT GGGGGGACCA 420
ACACCTTAGG AGAAGTGGAT CAGGGTTCTG CTTGAAGAAG CAGTCTGACC ATGCCTCAAC 480
AAAACAGCCA TGTTGTGCTG GGAAGCTGCC TCTGCTTCTG TAGACTTGGA CTCTCCAAAG 540
CCTGCAGGCT AGAATGGCTG AGTCATCCAA ACAACCAAGG TAGTGGCCCA CCCTTCCTCC 600
TCAGGCATTC CATCCCGGGA GAGATCAGAT TCCTGCTTAA AGAAGCATTC TGGCCAGGCT 660
CTGGCAAAGC AGCTGTGCTG TGCTAGGGAG ACACCTCCTC ATCTGGACTG TCTGACTCTC 720
CAAAGCCCAC AGTCTGGAAT GGCCAAGTAG ATCAAACAGC AGAGATGGCA CCCGCCCCTC 780
CCCCTAGGGG TTCAGTCTTG TATCAGGCAG GCTCCACCCT GTTGCTGGTG GCTTGCTGGA 840
ATTCCAAGCC AGTGGGTTTT ATCTTGTGAG GTGCCGTGAA AGTGGGGCCC ACAGACTGAT 900
GCTGCTCAGC CTCCTGGATT CAGCCCACTT CTTTGGGGTA TGCACGGACC TCCTGATTTG 960
CCTCGTTGCA TACACCTTTA TTAGAGATCC TGAGGCCAGA GTATGTAAAG CTCCTGGGTC 1020
TCTGTGTGTG CCTGAGCAGG CACTCTGCCA AGACTCCATA CAGCTCCGTG TGTTGAACCT 1080
AAGGCCCTGA TGGTGTGGGC TCACAAAGGG ATTCCCTGAT CTGCGGGTTG CAAAGATCTG 1140
TGGGAAAAGC ATGGTTTCCC AGGGTTGCAC ACTCACTCAC CACTTCCCTT GGCTGGGGGT 1200
GGGGGTTCCC TCGACTCTGT GTCACTCCTA GGTGGGCTGT CACCCCACCC TAGTTTTCTT 1260
TATTCTCCGT GCTTTGAGTT GTTTCCCTGA TCAGTCCCAA TGCGAGTATC TGGATATTTC 1320
AGTTAAAGGT GCTGTATTCA CGCACCTCTT TCGTTCCTCT CTGTGAATGC CACAGATCGC 1380
AGCTGCTTCT AATCAGCCAT CTTGGTCCCC 1410
|
