| Tag | Content |
|---|
EnhancerAtlas ID | HS098-51092 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:2613120-2614970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr7:2614238-2614249 | TGTGGATTGGG | - | 6.14 | | Nr5a2 | MA0505.1 | chr7:2613636-2613651 | AGATTCAAGGTCACC | + | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr7 | 2613591 | 2613991 | | chr7 | 2614028 | 2614116 | | chr7 | 2614357 | 2614426 |
|
Enhancer Sequence | AGGTAGTATT TCGGTTTGTT CTCTATTGAT TTGAAACGGT GAAAGCTTCC TATAACAATG 60
TATTAGAACA TCAGTGCCTG TGCTGGGAGG TGCCCAGATG GGAAGAGCGG GAGCGTTAGG 120
GTCGAACCTG AGTTTGAGCC GTGGCGTAGT GCCCTAGGAG CTGGTGTCCC TGGTTAAAGG 180
CCGTAGCACC AGCACATAAA AGGCAGCAGA GCTCATGTTC CATCCGTGCT CTGCTTCTCC 240
AGCACGATGG AGAAGACTGG ATGAGGACTA GATTAGCTTC AGAGTCGCCT TGCGTCCTGA 300
GATTGGGTAC TGTGATAAGG TCACTGGTAG AGTCATCAGT AACCTTCCAT GCATGCCACG 360
CTTTATGTTA TCAAGACATC TCACATGCCC TGTCTCAGGC CCTCTACAGA AGCTCTGTGG 420
GACGGGCAGA ACCACTTGTT ACAACCACAG TCTGCTGATG AACTTGAGAC TCAGCGACGT 480
TAGTGGTCTG TCCAAGGTTA ACCAGTAGCA GAACCAAGAT TCAAGGTCAC CTGCCTCCCA 540
AGGCCAAGAC TCTGTACTTC CCCATGGCCC CTCCCATTTA TGAAAGCATG AACTGCATTG 600
AGCTGTATCG TCATTGTCAC TGCCACCAGC ACCGTGACCA TCACACTGGC TTTCAGTATC 660
CGTAAATGTT TGCCCCTGGA GAAATCATCT GCGTTCATTT CCTTCCATAA TTTTAGTCTG 720
TTTATACAGC TACTGTCTCC ACCAGTTGAT GTGTGTCTGA GACACTGCGT TCAGTTGGGG 780
CACCAGAGGG CAATAGGGCA TTGGCAGCCT CGTCCCCAGA GCACGGAAGA GGATCTGGAA 840
GCCGTTTCCA TTGGGGAGCT GGGAAGAAAC TGGGGAACCT GGTGTAGACC ATTATACAAA 900
AGACAGCGCC TTCTCTGTTG GCCAGAGAGA ACAGTCAGAC TTGAGGCTGT GTGAGAAGAA 960
CGCTCTAACC ACGAGAGCTG TCTGACAGAG GCTGCGCTGC TGAGGAGCAA GTGCGCACCC 1020
TGGCCATGGA GATTTTGAGC ACAGGTGGCA GCTGTGTGTC GGGGATGTTA CAGAGGGGAT 1080
CCTCATTCCG GTTGGAAGAC TGCGCTGAAT GAACTCAGTG TGGATTGGGG GGATTATCTC 1140
GTTTGGGATT TTCTCAGTCT CTTGAATCTA TAGGTTTGTC TTTTGTTAAA TCTGGGACAT 1200
TTTCAGTCAT CAAGTCTTGA GTTGTTTTTT CAGCCTTGCC CTCTTTGGTT ACGGCTGCTC 1260
AGGTCCCTTG TCTCTGTTCA GTGTTTTCCC CTCCGTCTTC CCTCGTGAAG ATCGGGTAGC 1320
TTCACTATTC TGTCCTCGAG CTCACGGATG CTTTCTGCTG GCCTCTGCAT CCTGCAGTTG 1380
AGCCCGTTGT TTGTTGGGTG TAACCTTACT GTCTCGGTTC AGTTCTGAAA TCTCTGTGCG 1440
GCTCCTTCTG TCTTGGTCTT CGCTGAGACG CCCACCCTGT GCCTCTTCAC TTGTTTCAAG 1500
CGTGCCTGTC ATTGGTCACT GGCGCATCTT TGTGGCGGCT GCCCTAAGTC TGTGGCGGGA 1560
TTCCAATGTC CAGGCCATCT CAGTGTTGAC ATTATGGCTT GTTTTTCTTC ATTCAGGTTG 1620
AGCTATTCTT GGTTCTTAGT ATAAAAAGTG ATTTCCTTGA AACCAGGACG CTCTGAGTGT 1680
TTCATCGCGA GACTCTGACT CTTGCTCAAT CCTGTGTTGT GGCAGGCCTC CTTTCACGCT 1740
GCCCTGTAGG TCAAGGGGGT ACCACCTCGT TATCACCCGC GAGGGTGGAG GTCCAGTTCC 1800
CACTCAGCCA TCATCGACAC CTGCACCGGG AGGGGCTCCT CATTCCCACT 1850
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