| Tag | Content |
|---|
EnhancerAtlas ID | HS095-30350 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr8:145679800-145681430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chr8:145680803-145680813 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr8:145680803-145680814 | AAGGTGTGAAA | + | 6.62 | | TFAP2A | MA0003.3 | chr8:145680736-145680747 | TGCCTGAGGCA | - | 6.02 |
|
| | 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 |
| GH08I144455 | chr8 | 145681028 | 145682630 |
|
Enhancer Sequence | GGTGTGTGGG CTGAGGCATT CCAGGGCCAG CCAGGAGTGA CAGGGATGTG ATGTGCCTCC 60
CACCCAAAGA CTCTTAGAGC TCGCTGAGGG GAGCAGTCAG CAGAGTTGCT CCTGTCCTGA 120
TGCCTCTCCA GCAGCCGGCC CAGGCTTGCC AGCCATGCAA ACCTCCAGAA AGCCACTGGG 180
CTACAGGCTT CCTTTGGGAC CTGGGACCCT CTTGAGAATG GGATGTGGTG CAGCAGAGCA 240
GCCTGCCCAG GCCCAGCCTC TCTACAAGGT GTGTGTCAGG GAGGGGACAC TCACAGGGCC 300
CTGCCTGGTG GCGCTGGGAG GCCGGCCCTG CCTGGTGGTG CTGGGAGGCC AGCCCTGCAC 360
ACGTGGGGCC CTGGGAAGTC TGAGCTGCCA TCCTACTGCT TCAGCTGCCT GTGCACCCCA 420
AGCTAAGGAG CTGTCAGACG CTGGGGCTGT TCACTCAGCA CCTGTGGACT AGGCCTAAGG 480
CCTGCTGAGT CAAAGGACCT ACATGTGGAG AACCGACAGT GAGGACAAAG CCCTCTTTCA 540
TGGAATCCAC ATCCACATGA ACACCACCCG TTACCTGCAT TCAATCCTCA AGTTCTCAGT 600
TTGGTTAAAA ATTAAAATTA CAGGCGGTGG CTCATGCCTG TAATCCCAGC ACTTTGGAAG 660
GCCGAGGCAG GCAGGTCACC TGAGGTTAGG AGTTCATGAC CAGCCTGGCC AACATGGTGA 720
AACCCCATCT CTACTAAAAA TACAAAAATT AGCCATGCAT GGTGGCGAGC GCCTGTAATC 780
TCAGCTTCTC AGGAGGCTGA GGCAGGAGAA TGGCTCGAAC CCGGGAGGCG GAGGTTGCAG 840
TGAGCCGAAA TGGTGCCACT ACACTCCAGC CTGGGAGACA GAGTGAGACT CTATCTCATG 900
AATACATAAA TAAATAAAAA TTAAAACATA CACAGTTGCC TGAGGCAGGG AGTGAGACTG 960
GCTCTGACTG GGTTGGGGAC AAGCTGAGAC CTGCCCCCAG GAGAAGGTGT GAAAATCCGC 1020
CAGCCAAGTC CAGGGGTCAG TGGTGGGTGG ACTACAGGCA GGAGGGGGCA CAGATGCTAT 1080
TGAAGCAGCT GTCCTGTGGG AGGCACAGAC CAAGGGCCCA CACCACTGTC CTCTCACAGC 1140
CCCCCGCCCC CCGGAGGTAT GCCACTCCAC GTGGCCAGCT CTAAACACCT CCTGGTGAGA 1200
CTGCCGGGGG CCTTGGACGA GGTTCTGGGT CCAGCTCTGC ACGTACAGTG GCCTTAGCAC 1260
AGGCAAAACA GCACTCTTCT TGGCTGTGGC CCGACCCCCA AGGGAGTTCC AGGCAGGGCT 1320
GGAGCATCTA ATGCCACCCA CCAAGGCCAC CTGGCCTCTC TTCCTGGCTC TGCATAGCCC 1380
AGGAAGATTC GAGGTGGGGT CCTAGACCCT CCTAAGGGAG CACTGAGGCT GCCAAGCACA 1440
TCACCACTTA CCTCCCAGCA CTGCGGGCCT CTCCCCCGAA AGCCACCCCA GCTCCTGGGC 1500
CGGCCCCTGG CCACAGGCCT CATTCCTTTG GGGCCTCCAG ATCCCAGCAT GGGCTCAGTC 1560
AATTCCATAC CATGAGGAGG CAGCAGTGAC CCTGCCCTCC TCTGGCTCTC TCTGGGCCTC 1620
CAAGAGGACC 1630
|
