| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06211 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:107153350-107154380 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:107154069-107154090 | AGCTCCTCCCCTTCCTCCCCT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 107153400 | 107154200 | | chr12 | 107153976 | 107154194 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I106757 | chr12 | 107151408 | 107154870 |
|
Enhancer Sequence | AGGCCTGAGG GTCCACCACT GCTGCCACAC AAACAGCATC CTGTAGGTTC CCATGACGCA 60
GAGCACAGGG GTATGCGCCA GTGTTTCTGA TCTGATTTGG GATTAGGAAA GCCTTGGCGT 120
GCTGTCCATA GTCTCCTTGG CAACAGCCCT TGGTGCCTTC TCCCTTGAGT TCCCAGACAC 180
CACCTACGCC CTTCTCCCTC TTTCCTAACT GTTCTTTTGG TTCTGAAGTG GCTGTACTTT 240
TGCTATGTAA GGCATGCCAT CCTATGTAGG GGGAAAAATC CCTCCCTACT CAAATTGGGA 300
TCCCTCTTTC TTGACCTCTG AATTGCTGGT TCTCTTTGCA TGCTTCCGGC CTAAGCGCCT 360
TCCCCAGCTC CCCTTAGGCT CTCACTCACA GAGGAAGAGC AGTTCCCTGT AGCCACCTAG 420
ACTCCAGGGA GCAGCCATTG TTGTCATAAC CCCTTCTCCC TGCTGTCTAG GCTTCAGCCT 480
GTCTGTCTCC CTCACAGGAG GCAGCCTCCC ACCTAATCCC CTGGGCCTCC ACTTTCCAAC 540
TGTCAGGGAA GACAGATGGG GAGCAGAAGA ATTCATACAT TCACACAGTC TCTCTCCTCC 600
TCGCTGCTCT GGCCATCCTT GTTGATTGGC TCCTGTCCTT GTTGGTGTAG CCCTCAGCAC 660
AGCAAAGAAA TCTTTGTGCT GACTGGCCTG CAGACTGGGA GCTTTCAAAG GAAGCCCATA 720
GCTCCTCCCC TTCCTCCCCT CTGATCCTAC TAACGGGCTT ATTTGCATAG CTGTCTTGGT 780
AACAGAAAAG AATGTAAAAG AAGAAGCACT TCAGAAGCAC TTCTCTTACT CCTAATCCTT 840
TCTAGAACTA CTTCCCCTCT TCTTGTAGCT ACTAACACCT GTTCCTCTGA CCTGCACAAA 900
AGCTCCCCTC CCCGCCCCTC TCAACTGGTT TCTCTTGACT CCTTCCTCCA CATTCACACC 960
AAGCCCAATT CCTATTCATG TATCTTCCAG GAGTTCAGTG AATGTGAGCC AAAAAGAAAA 1020
ATGTTCTCTA 1030
|
