| Tag | Content |
|---|
EnhancerAtlas ID | HS047-31883 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr7:143168460-143169970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr7:143169618-143169639 | TTCCTCATCCCTTCCTCCCCC | - | 6.69 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 143168830 | 143168932 | | chr7 | 143169270 | 143169864 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I143471 | chr7 | 143168560 | 143170401 |
| Enhancer Sequence | GGAGCATAAA AGACTAGGAT GGCTACATAG AAAAGCACAG GAATCATTTT ACCTTGTCAG 60
TCCTTCCCAC TGTTTGGCAC GGCTCAGTGC CAAAAGGGAT ACATTTAGCT GCAATCTTTC 120
CCCATTGGGG TAAAGGAGGG AAGGAGGATC TCAACAACCT TCAACACTGA GGACTCCAGC 180
AGCCTTTGTT GTAACCACAG ACACCTGCAG CTTTTCCCAC TAAGGACCGT TGCAGTTTTT 240
GCCAATGATG ATTCCAGCTG ATGGAGCTAT CCGGAGTCCA TACCATGTGA TACTCCTCTC 300
TCACACTGGG CCCAAATTTA CCATACTACC TTGAAGTTGG AGCTACCATT TCTTCTACCC 360
CAATGTGGGA GCCGCTGCAT GCCACCCTGC CAGCACCCTC AAACCCACCC ATATATAAAG 420
TTCTTTCTCC ACCAAAGCCA GTTTTTAGAG TTTAGAAAAG GTTACTGCTC CTTCAAGTGT 480
GCAGTCATCA ACCTGAGGCT AAAAGGAACA TAAAAAACCA AGGAAACATG ACATCACAAA 540
AGAAACACAA TAAATTTCCA GTAACCAACC TCAAATAATT GGATATATAC AACCTACCTG 600
ACAGAGAATT CAAAATAATT ATTTGAAAGA AGCTCAGTGA GCCACAAGAT AACACAGACA 660
ATGCAACAAT ATCAGGAAAA TAACACATAA ACAAGTTCAA AAAAGATCCA GGAATCATAA 720
AAAAGAACCA TACAAGAATT CTAGAGCTGA AGAATATAAT TAATGAAATG AAAAATGCAA 780
TGGACAGCCT CAACAGCAGA CGTAATTGTG GGAAAGAGAG TTTCTGGGGT GCCAGTTGAA 840
TTGGTCTCCC CTGTGTGAGA CACCCATGGG CTGCCCGAGA AAAGTCTCCT TATTGCCTTC 900
ATGTCTTTAT GCCCCGAGAG CATAACGCTC AGCGGCATTC CACAGGTTGC TCAGGGAGAT 960
AACACTCCCT TGAAGCAGTG GAGTATAATC AAACAGCTTG GCTCCTCCTG AAACCTGCTC 1020
CCACCAGTTT CAGTCCTGAT AAGTTAAAGA TCTTAAGTAG TTTAGACACA CACCTTTGCT 1080
CAAGGAAATT CACAGAAGCC GCCACTGCTA TACATCTTAT CGAATGACTC ACAAGTTCTC 1140
CTTCACTGAT TCATCCTTTT CCTCATCCCT TCCTCCCCCT CCCATCTACC CTAAGAACAA 1200
AGAGCTTGTA AACCAATAAA TTGGGTGGAG CCCGAGAGCT CTGGGCCGTG AGCAAGCCTC 1260
CAACGCTCCA GTCCCCTGGA CCCACCTTTA AAACGCTTAT TCTGTCTCTT TCTAACTCCT 1320
TTGTCTCTGC CGGACTCGGA GTACCCGCTG GGTAGTGTGG GGCTGGTTTC CCCAACACTT 1380
AATCAAGCAG AAATCTGCAA ACTGGAAGAC AGATCATTTG AAATTATCCA ATCATAGAAG 1440
AAAATAGAAA AAAGGAATGA AAAAGAGTAA AGAAAACCTA TGAGATTTAT GGAACACCAT 1500
CAGGTAAACA 1510
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