| Tag | Content |
|---|
EnhancerAtlas ID | HS105-51682 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr21:38155880-38156930 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr21:38156835-38156850 | TGAACTCCTGACCTC | - | 6.22 |
| | | 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 |
| GH21I036783 | chr21 | 38155974 | 38157134 |
| Enhancer Sequence | GGAAAGGAAC AAAGAACTGG CATTCGGACA CAAAGTGTGC ACCACAAAGT GCCATTACGT 60
GCAAGACAGC CACTTAGTGT GTCTGAATCC CTGTTGGTGT TCTGTCTCCC TACAGTGGCT 120
TCATTCGCGA TCACCAGATG TCAGGTCTGC CAGATGTCGT TTTTAGCACC ATGAAGCATA 180
GCAAGGGCTG GTGTCTCGCA CACACACAAG CATGTGTGCA CATGCACACA CACACATGCA 240
CATACACACA CACACATACA TGCACAAATC CACACACACA CACACTTGAT TGCCACCTCA 300
ATATGGCAGG CTTCCAACAG TGAGCACACC AGCCAACATG GCACCATCTT TCCACTCACT 360
GTAAGATTTC TCCAAGGTCT TATAAATGAA TGAATGAACG GGCCATGGGG AAGGGGTATC 420
TTCAGCTATA GATCTCAAGA TTCTACACTG CAAGCAAGCC AGTGGTTCCT TTGACTGAGC 480
ACCCATCCAC ATGCTGGGCC CTTGGTATGA GCCATGTTCT CATTTAAATG TCCCAGTGAC 540
TCTCAAGACA TCATCATTGC CAAGTAGTCT CATTTTACTG CTGATAAGTG GAAGCTACAC 600
CGCAGAAGTG GCCTGGTGAG ATCAGAGAAC AGTCAACCAG GTTTGCCTGG CTCAGAGGCC 660
CATCTTCTGA CTCACTAGGA AAGAATCTTT TGCTTTTATC AAAACAGAAT TTCAAGGTAG 720
AAATACCACC TCTTTTTTTT TTTTTTTTTT TTAATGAGAC AGAGTCTTGC TCTTCACCCA 780
GCCTGGAGTG CAGCGGCACT ATCTCAGCTC ACTGAACCCT CTACCTCCCA GGTTCGAGCA 840
ATTCTCGTGC CTCAGCCACC TAAGTAGCTG GGACTACAGG CATGTGCCAC CATGCTTGGC 900
TAATTTTTGT ATTTTTAGTA GAGATCGGGT TTTGCCATGT TGGCCAGGCT GGTCTTGAAC 960
TCCTGACCTC AGGTGATCCA CCCACCTCAG CTTCCGAAAG TGCTAGGATT ACAGGCGTGA 1020
GCCACCATGC CCGGCCGGCC AGCCTCTTAA 1050
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