| Tag | Content |
|---|
EnhancerAtlas ID | HS051-25198 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr7:97830600-97832880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SCRT2 | MA0744.1 | chr7:97831730-97831743 | GCACCTGTTGATT | - | 6.16 |
| | | 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 |
| GH07I098202 | chr7 | 97831487 | 97833013 |
| Enhancer Sequence | ATCTGAAATG CTTAGGACCA GAAGCATTTT AAATTTCTGA TTTTTTCAGA TTTTGGAATA 60
TTTGCATTAT ACTCACCAGT TCAGCATCCC AAATCTGAAA ATTTGAAATC CCAAGTGCTC 120
CAGTGAACAC TTTGGGCGTC ATGTCAGCGC TCAAAAGGTT TTGGATTTTG GAGCATTTTG 180
GATTTTTGGT TTTCCGATTT GGGATGCTCA AGCTGTAATA CATGTTTTAT CCCTGGCTGC 240
TTTCAAATCT TTGTCTTTAG CTTTCAGCAG TTTGATTATG GTGCATCTGA GGGTGGATTT 300
CTTCGTGTGT GTGTTTTGTT TTGTTTTGTT TTGTTTTGTT TGAGACAGAG TCTTGCTCTG 360
TCACTAGCTG GAGTACAGTG GCACGATCAT AGGTCACTGC ACCCTTGAAC TCCTGGGCTC 420
CAGTGATCCT CCCTCCTCAG CCTCCTGAGT AGCTGGGGCT ACAGGCGTGC ACCACCACGC 480
CTAGCTAATT TTTAAATTGT TTGTAGAGAC AGCATCTCAC TGTGTTGCCC AGGCTGGTTT 540
TGAACTCCTG GCCTCAAGGG ATCCTCCTGC TTCAGCCACC CAAAGTGCTG GGATCACAGT 600
TGTGAGCCAC CCCACCTGGC CCAATTTCTT TGTATTTATC CCGTTTTTGT TTTGCTAAAC 660
TTAAATCTGT AGTTTTGTAT CTTTCACCAA ATTTAAGAAG TTTTCAGGCA TTCTTTTCTT 720
CTAGTACTTT TTCTGCCCCA CGCCCTGTCT CCTCTCTTCC TGGGACTCCA GGGTTAGACC 780
CTGTGTATTC TCTCATAGGT TCTGAGGCTC TGGTCCTTTC TTCCTCCAGG TTTTTTTTTT 840
CTTGCTCTTG TTTGGATTGG GTGATTTCTG TTGCTCTGTC TTCAAGGTCC CTGATGATTT 900
CCTTCGTCAT CTCCATTATG CTGTTGAGCC CATCCATTGA ATTGCTAGAT TTTGGTTATT 960
ATACTTTTCT TTTCTGAGTT TTGCTTTTTG TCATTCTTCT TATCATCTGT TCCTTTGCTA 1020
AGATTTTCCC TATTTCTGTT CATGGTAAGA GTGTTTCCCC TTAGTTGTAG GAGCATTTTT 1080
ATAATAGTCC TTTTTCAGAT AATTCCAACA TCTGTGGTAC GGTGACACTG GCACCTGTTG 1140
ATTGTCTTTT CCCAGGTAAA TTGAGGTGTT CCTGGTTTTT GTATGTGAAG TAATTTTAGC 1200
TTTTGGATCC TCCTATCATG TTAGGCAGTC TGTGCCATGT GTAAATGCTG TGAATCATGT 1260
TGATACTTTT ACCTTAGCAG GCCTTGACCC GGTGGGTGCA GGCCACAAGC TCCAAGCAGC 1320
CTTCTGTGGG TTGTGGTTTC AGTGTCAGCT CCCAGTTCCC CTTTCAAAGC CTTCGCTGTG 1380
CTGTTTGAAC CTGCCCCACG TGTGTGCCCC GCACCCCACC CCGGTCTCCC CTGAGGTTCA 1440
TTTTCAAAGC TTGGGTGTGT TCAGAGTCAG ATCTACCACA CACAGCCCAG GAGCCCCCCA 1500
GCAACTTCAT CGGGTCACCT TTTTGAGCTC CTCCCTCTTC TGTGATGTCC CTGATACTTG 1560
CAGTTCTTTG GGCCTCTGCT TTCTGGTCCC CTAGCTAGAA AGTTGAGGCT TTAGTTACAC 1620
GATGTGCCAT ACTTCCTGCA ATCGCACGCG CATCTGGAGC CAAGCAGTGG GAGGACAGAA 1680
GGGAAAAAAA CTCAGCGAGG GTCCCCTCCC GCTCGTGATC ACAGTCCTCC AGTGGAGAGG 1740
AGGCTTCATG GCCCTCAGGA TTATAGGCAG CTGTTGCCCC AGGATTGCTT GAGACTGGAG 1800
AGCAAGAGAA CAGAGAAAAG AAGAAAGCTG GAATTCCCCC TTCTCTTTCT GAGCATCAGA 1860
AGACCCCCTT CCTGCTCCGA AGCCAGAACC AAGGGCTTCT CCTGGAGCAC TGTGTCCAGG 1920
GCAGTGCCCA CTTTGGATTC CGGGCTGACC TGAGTCCAGG CGGGGGATTG TGGAGGAGAA 1980
GCCGACACAC TTGTTGCTGG TGGGTGGCAC CTTGAGCACT GCCGCTCGTG CCCGCCTGCC 2040
TGCTGCTCTG CGCTTCTCTG CAGCCTCAGA GGGCTGCTTC ATGCCTCTGC CGAGGTCAGA 2100
GCTGCAGGCA GAGGGAGAGA CAGGGCCTAG TGTCTGTCCG TCCTCCCAGG CCTGGAGCCG 2160
CCCTTGTCTT GAGACGCTTA CTTCTCAGTC GATGAGTCTG ATGCGCCTGC CAGTGGGGAA 2220
GCGGTCACAC GGGGGGTTCC CGTGAGCAGG CCTTTGCTGA CAGGAGTTTC TGTTTGACTT 2280
|
| |
|
|
|
