| Tag | Content |
|---|
EnhancerAtlas ID | HS138-16064 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr17:5458110-5459590 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr17:5459196-5459211 | GAGGTCAGGAGTTCA | + | 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 |
| GH17I005554 | chr17 | 5458144 | 5459444 |
| Enhancer Sequence | GCAGGAGGAT CGATTGAGCC CAGGAGTTTA AGACCAGCCT GGGCAACATA GTAAGATCCT 60
GTTTCTACAA AAAATAAAAA AAATTAGGCA ATGTGGTGGT GTGCACCTGT AGTCCCAGCT 120
ACTCAGGAGG CTGAGGCAGG AGAATGGCTT GAACCTGGGA GGCCAAGGTT GCAGTGAGGT 180
ATGGTCATGC CACTGCACTA TTCCTGGGAG ACACAGTGAG ATCCCATCAC ACACACACAC 240
ACACACACAC ACACACACAC ACACACGAAA AAAAGCCATA AATGAAAGCT TACTTGAATT 300
TCTTTTACAC TTACTTAGTT TTGTGAAACT TGAAAAATAC ATTTTAAATT TTTTATTTCC 360
GTTGGCATTT GCCATCCTTA ATCAAGGTGA CTGAAAAAAA ATTAAAAATT TATACTTGAA 420
AATGCACAAT GCTTAATCAC ATGCCAAACA CCTGGAAGCT CCCATCCTGT CATCTTCATT 480
TCTTTAATAT CTCTGGTTGG TTCTCCTCTT CCTTCACACA GCCCTTGGCC AACCTCCACC 540
CTTTCTTCCT GAACTTTCTT GTTTTTTTTA TAGTAGCTTC CTTATTCTTC TCTCTGCCTT 600
GTCTAGCTGA TTCAGTTCCT TGAAAATTTC TCCTCCCACT TGTGGCTGAA GCCTCTGACT 660
TTCCCACGGC ATTCTCTTAA GGCTCCACTT GCTCCCGCCC ATCCCAAACT CTCCTCTCTG 720
GCCTGGTGTT CTTGGTTCCC TTTGCCTATC CCAGCCCCCA TCCCCCGGCC AGCCACCATC 780
TGGTCTCTGC CTCTAGCTGC TTGGAACTCT TTGAAGATTT CCCACCTGTC CACTGCTACT 840
TGCAGTACCT GTATCCAGGT CCTTTAAAGC CTACCTCACA TTTATAACTA TGAACAACTA 900
GAAGCAGCTT AAAATGGCCA AGAACAGGAG AATGGTCAAA TCAGCCATGG CACTTTCCCT 960
ATGGAATAGC ATGTGGTCAT TCAAAATGGT GTTGTATCAG ACTACTTAAA AATATATAAA 1020
GGGCTGGCAT GGTGGCTCAT GCCTGTGATC CCAGCACTTT GGGAGGCTGA GGCAGAAGGA 1080
TCATTTGAGG TCAGGAGTTC AAGACCAACC TGGCCAACAT GGTGAAACCC CGTTTCTACT 1140
AAGACGACAA AAAATTAGCT GGGTGTGGTG GTGCGTGCCT GTAATCCCAG CTACTCTGGA 1200
GGCTGAGGCA TGAGAATTGC TTGAACCTGG GAGGCAGAGG TTGCAGTGAG CAGAGATCGT 1260
GCCACCGCAT GCCAGCCTGG TGACAGAGCA AGACTCTGTC TGTCTCTGTC TCTGTCTCTC 1320
TCTCTACACA CACACACACA CACACACACA CACACACACA CACACACACA CATGAAGGGC 1380
TGGGCATGGT GGCTCACATC TGTGATCCCA GCACTTTGGG AGGTCAAGGT GAGCAGCTTG 1440
CTTGAGCCCA GGAGTTTGAG ACCAGCTTGG TCAACACAGT 1480
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