| Tag | Content |
|---|
EnhancerAtlas ID | HS191-03594 | Organism | Homo sapiens | Tissue/cell | Trophoblast | Coordinate | chr1:228124420-228126160 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:228124563-228124576 | TTCTGGAATCTTC | + | 6.2 |
| | | 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 |
| GH01I227937 | chr1 | 228124828 | 228124930 |
| Enhancer Sequence | GACTCAAGTG ATCCTCCTTC CTTAGCCTCC CAAAGTGCTG GGATCACAGG CACGAGGCAC 60
TGTGCCCAGC ATGCTGTGTG CTTCTAATGT GTCATGTTCC AGGGTGAACT TATTTTTACT 120
TTTGGCCTGG GAAGACACTG GGCTTCTGGA ATCTTCTTTA CAGCTTTATT CAATTTCGGA 180
AAACTCTCAT CCTCTCCCCT CATACATATC AGCCCTGTCC CACTCCCGCA CCCTTCTCAG 240
CTGCCTCTGG CATGGCCTCC CCGTGTCACC GAGGTGTCCT GCCCTCTGTC TGACATCTTG 300
CCGCCTCTCT GGTATACTCT GGGTAATTTC TTCTGACCTA TCTTCCGTTG TGCTAATTCC 360
CTTCAGCTGT TTCTAATCTG CTTTTAAATC AGGCCTTACT TACTTTTCTC CCCCTCTAGC 420
TCTATTTGGT TTTTCCAAAC TTGCTGGGTC AGTCTTTGTG GTTTCCCGAG CCTTGCAGCC 480
ATCCCCAAGT GTCTTCCTTC CTAGAGGCAG AGTGAGGAGA GCCGCTGCAC TCAGCACCGC 540
TGCTCCGCTT CCTGGGCTGC GGCTGTCTTT TCGAGGCCCC TGTTGTGTTT CTGTGCAGGC 600
CTGGTTAGCT CTGACCCCGG GCTGCTCACT GTACTGAGGA AACAGTTGGC AGAAACAAGT 660
TGAAGGAGAG GATAAAGGTA CTACAGTAGG TGGAATGGTG TCCCCCACCA AATGCGTCTA 720
ACGCAACCTC AGTCAGGGGC CTTATGTGGA ATAAGAGGCA TTGCAGAAGT AACTGAGATA 780
AGGATCTCAA GGCAAGATCA TCCCAGACAT GGTGGGCTCT TTAGAGCCAG TGGAGGCTGT 840
CCTTATAAGA AAAAGGAGAA GACACAGAGG CGGACGAGAG GGCCACGTGA AGATGGAAGC 900
AGGGCGTAAA GTGGCCAGTC AACCAGCCAA GGAGCCCCAC GGTTCGCAGC CATCGCTGGC 960
AGCTGGCAGA GGCAGGAAGG ACCCTCCCCT CAAGCCTCCA GAGGGGCATG GCCCTGCGGA 1020
CGCCGTGATT TCAGACTTCT GGCCTTCAGA CCTGAGACAG AAGTCCTGTT GTTTTAGGCC 1080
AGCCAGTCTG TGGTGCCTGA CAGCAGCCCC AGGACAGCAG CACAGATTTT GGAAAGGATC 1140
TCGTTATGTG CACACCAGCC AGGCTTCTAG GGCCACCTGC GGTCCCAGAG CCAGGCCACC 1200
CAAAACCCAG CATGAGGCCA GGGCCCGGGA CCACGCTGGT GACTCAGGCC TCAGCGCACA 1260
CGTGGTGGCT GTGCCCTGCC CTGGGGGCCA CCTGGGACTG TGGGAGGGCC TCCTCTGAGT 1320
ATTCTCTCCT TAGCGGGTCC TGGCCTTTAC TATGCACCCT CATCCCATGA GACCAAACCA 1380
ACCTCACACT TTCTTGTTCA GCATCTGTTC TTGCTATTTC TAGGGATCCC CACCAACCAT 1440
TTCATCAGCT CTTTGACACT TATAAAGTTA AATATACACA CACACACAAA CCCCCCCACA 1500
CAGATACACC CATACACACG GACACACATG TGTACACACA CACCCCCATA CAAACCCATA 1560
AACCCATACA CACACGCATA CACACACACA TATACCCATA CATACACACC CATACAAACC 1620
TATACACACA GACACACGCA TACACACGTA CAGGAACAAA CACACCCACA CAAACCCCCT 1680
CACACACACA CACACAAACA CACCCATACG AACCCATAAA CCCATACACA CAGACACATG 1740
|
| |
|
|
|
