| Tag | Content |
|---|
EnhancerAtlas ID | HS047-32683 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr8:41605000-41606300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr8:41605602-41605614 | GGTGACGTCAGC | + | 6.14 | | CREB1 | MA0018.3 | chr8:41605602-41605614 | GGTGACGTCAGC | - | 6.14 | | FOS | MA0476.1 | chr8:41606140-41606151 | TCTGACTCATT | + | 6.32 | | IRF1 | MA0050.2 | chr8:41605411-41605432 | GAAGGGAAAATGAAACCAGTC | - | 6.71 | | IRF2 | MA0051.1 | chr8:41605415-41605433 | GGAAAATGAAACCAGTCT | + | 6.17 |
|
| | 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 |
| GH08I041747 | chr8 | 41605273 | 41605943 |
|
Enhancer Sequence | AATTGCATTT ATCTGCGCTT GTGCCTGTCT ATCCCAAAGG CCTGAATTCT TTGAGATCCT 60
GTGTTTTGCT CACCTTGGTA ATCAGGTCCT AGCATGGAGC CTGGTGCATA AGGTTTGCAG 120
AATTCAATGC ACCTTCATGG AACCTGCCAC ACACAGGCCT ATCTTTTTTC TTTGTCTCTA 180
AGCACTATGA AGATCATGTC TAGTCTTCAT ATTCTAAATT CCTAGAGCAA TGAAACCATA 240
ATGTGGAGTT TAGAGAGTGT GTGTTCCTTG CACTACATTC CGGATCGTTC CTGAAGGTGC 300
TAGTCACCCT TTTCCCAGTC CCTAGGATTC CATGGAATGT CCCTGCTGTG ACTACAAATG 360
AAGATTTTTA TGTAACTGAA CTGGTCAATT AGCTCTTCCT TGGCTGCAGA GGAAGGGAAA 420
ATGAAACCAG TCTGGGGCAG ATCACCCAGA GCAATAACAG GCTTGCTGCG CAGTGTCAAA 480
TCCATCCTCT GAGTCAGTAC AGAGGCTTGG GCTGGGTGTC TCAGTCCTGG GCTCTGAGAC 540
TCTTCACCTC TCTGAGTCTC CCCAGCCTCC CTGGTCAAGC ACCTGCTCTA ACCAACTCTC 600
AGGGTGACGT CAGCATTAAC GGTGTCGCAG GTACCAGGTG CCAGGCATAG GGGCACCTAG 660
CTGCATATCT GGTTTAACTA TTTAACACAG AACACTCTTC TCCCAGGTGA GGGCTCCAAT 720
GAAACGTTCT TTCTTCCTCA TCCCTATTCC AGAGCTGCAC CAAGGCAGCA AGTCTAAAGA 780
AGTTTAATAC CACAACACCA TCATTTTAGG AAGGCTTTCT GTGTGTTTTC GGGGTGCAGC 840
TAGGATCAGA GAACTATGTA GTTTAATACA TTTTTCTATG CCTGTCAACA GTTCCTAAGA 900
AAAAGACAAT GACAGAGAAA AGTGCCAGGT TCTAGATCTA TACAGATCTA GCTCTAACCT 960
CCTTAGCTGG ATTGACCACC ATCCTCACCC TCTTTCATTT CATGTACCCC AACCTCCCCG 1020
AACTGCCCCC TGCCCCAGTG CCCTTTGGCA CTCCAGCCTT TGCAGTCTGT TCCTTCTCAC 1080
AGCAATTCCT GTTTCCCAGT TCTGTACTCG GAGACTTGTA TCCTTCCTTC ACAACCTTTC 1140
TCTGACTCAT TAGCAAGCCA GCCACTACCC TTAGACAAGA AACGACATAA GGGCAGGTCC 1200
CAGGACCTGC TCATCTTTGA CTGGCTGGCT CTTGGAACAT TAGAACAGCT CAAAAAATAT 1260
TTGTTGAATG AAGCCAGGCG CGGTGGCTTA CGCCTGTAAT 1300
|
