| Tag | Content |
|---|
EnhancerAtlas ID | HS112-01209 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr1:182708180-182709670 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr1:182708834-182708849 | CTTGGCCTTGACCTC | - | 6.3 | | RREB1 | MA0073.1 | chr1:182709098-182709118 | CCAACACCCAACCCCCAACC | + | 6.01 | | TBX20 | MA0689.1 | chr1:182708854-182708865 | CTTCACACCTC | - | 6.02 | | TEAD1 | MA0090.2 | chr1:182709078-182709088 | CACATTCCAT | + | 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 |
| GH01I182738 | chr1 | 182707891 | 182709380 |
|
Enhancer Sequence | AAATAAAGAA TCTTATTGGA TCCTCTCCCA GGTATCTTCT AGCTGACATT TATGGCTTCT 60
TTCCATTTAA AAGTGGAATA TTCCCCCACA AGTGTGCTGG GAAAGTCTCA GCTTTCAGAT 120
GAACAATGAA ATATGCTGGA TACAGTCAGC TGCTACTTGG CTTCACCTTC TGCTCTTTCT 180
CTAGTGTCAG TACTTACTCC TCATCTAGGA AGAGAATCAG TGCTTAACGT GAGAGAAAAA 240
GAACCCAAAA GATGGCTTTC TGAGGGGCTT CGCACAGCCT GATAAGACAA TGTATTTTCT 300
CCCCAACGCT GTCATCTGGG GAAACACTGT CATCCCCAAC AGTGTCACTG GGGCCCCGAC 360
CTTGAGTACT GACGTGGGGG AACTGATGTT CTTTCAATGG GGTTTTTAAA GGCACACCAG 420
CAGTCACAGG CATACACACA GTTTCTGGCA TTTATGAAGA ATTGGGGTTT CTTTTAAGAG 480
GAAAAAAAAG AATAAACCAA ATTGTTCATT CCTTTTCTAA AGTATTGTAT ATTGGCTTTG 540
TATTTGAGGA CTGCCTTGTT ATCTTCATGT TTTCAGGCCT CCCCCTGTCC CATAGCCTAG 600
GGGGAATCGC CATGGCCCTG ATTTGTGTAT GTAGACAGTG CTGTTTCCAT TCCTCTTGGC 660
CTTGACCTCT GCCTCTTCAC ACCTCCTCCC ACTCACCCAG CCAGCGGGCA GCCCACCCAG 720
AAGCCCTTGC GCCAGCAGTT ACCTGGCAAC AGCGACAATC ACGCTAACAG GCAGCAACAC 780
AGCAGCAGAG ACCAGAGAGC TCTGAGTCTT CCAGAATCTA AGCAGGGAAG GGAAGGGGGG 840
CAAACGGCTG TTTTTATCAA TGGCTTTTCG TCCCTACCCA TACTGTTTTC CTGTCTCACA 900
CATTCCATGC TCCAGCTCCC AACACCCAAC CCCCAACCCC CAATTTCTAT CATCGCCTGG 960
GTGAAACTAG CCTCCAATCC AGAGTTTAAT AACAGCCACA GAGATTCATA TGGAATTGTG 1020
TACTTGGGGA GACCCAATAA TCATCCCCCT TAATTCCAAT GCAGAATGCT CAGGAGTTAA 1080
TCAATCCTAG TTTCCATCTG TGCACATGTT GTGTTGCAGT CCAAGGATGT ACTTGACCAC 1140
CCAACTGGCC TGCTGTAATA GAGACCTAAG TGCTGTGTAC TCAGAAACAT TGACAAGCTA 1200
TTATCTTACT TCTTGCCTCC CTGGCCACAA TTCTACAGTA AGTGCTACCA GAGAGTGGGG 1260
CATAAGCATA CCAGTTAGTA ATAGCTAATA TTTACTGATA CTTATTCTGT TCTAGGCTCT 1320
GTGCTGAGCA CTATACAGAC ACATCTAACT TTCAAAACAG CCATATGAGA TAAATAATAT 1380
TACTATCTCC ATTTTACCAA TGAGCAAAAC TGAGGCATCA AAGGTCGTAC ATCTATTAAG 1440
AGCAGGGTCA GAATTTGAAC TCATTTCAGG ATTTGAACTC ATGTTGTTTT 1490
|
