Tag | Content |
---|
EnhancerAtlas ID | HS049-01294 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr11:34213180-34215670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr11:34214613-34214625 | TGCCCCCAGGCA | - | 6.04 | ZNF263 | MA0528.1 | chr11:34215434-34215455 | GCTTCTGCCCCTCCCTCCTCC | - | 6.83 |
|
| 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 |
GH11I034191 | chr11 | 34213531 | 34215570 |
|
Enhancer Sequence | CTTCCTGGAC CCTCTGCTGC CCTTATTCTT AGAAGGGTTC AGGCCCCAAG AAGGGAAGTG 60 TGGGAAGAAG GACAAATAAA ACCCAGCCAA TCACAAATAG CTGCACCAAT GGGGGCAGGA 120 CCTTCTCAGC CACAAGCTCA GCCCTGTGTG TCTTGGCCAA CAAGGTCCGC CCACTTCTGT 180 GCTCCATCCT GCACAACAGT GCCCGTGTTC CCTTGCTCTG CTCCTCCCCA TCGCCGGTCT 240 CTCTGGGGTG CCTTGCTGCC TCTAGCCACT TGGACTCTGT ATATGCTGCT CCCCTGCCTG 300 ATACAAACCA TCGTGCTGAT AATCATAAGA ACAGATACTC AGTGTGTCCT AGGCCCTGTT 360 CTAAAAGTAT GTAGTGAGCA GGTGCAGTGG CTCATGGCTA TAATCCCAGC ACTTTGGGAG 420 GCCAAGGCAG GAGGGTCCCT TGAGCCCAGG ATTTTGAGAC CAACCTGGGC AACATGGTGG 480 GACCCCATTT CTACAAAAAT TTTTTAAAAG TTAGCCAGGT GTGGTGGGGC ACATCTGTGG 540 TCCCAGCTAC TGGGGGGGCT GAGGTGGGAG GATTGCATGA GCCCAGGATG TCAAAGAGGC 600 AGTGAGCTGA GATTGTGCCA CTGCACTCCA GCCTGGGAGA CAGAGCAAGA CCCTGTTTCC 660 AAGAAAACCC CCCAAATATG TTAACTCATT GGGTCCGCAT ACCTTACAGA TGATTAAGAG 720 CCTTGAAGAG GTTAAATGAC TGGTTGAAGG TTATAAAAAG TGGCAAGGTA GATCTCAAAT 780 GCACGCCTTT GAATAGCAGG GCCCTCCTCA GATGGGGCTA TTCTGGCTGG CTACGAAGTC 840 ATGACACCAG AGGTTTCTAG GCCCGACCCC CAATCAGAAC TCTGGGAAGG GTTCCACACT 900 CCTCCTGTTT TCATGTCCTG GATACCAGCA GGCTCCAAGC CTTCTGAGTG TGCCACCCTC 960 CACAGAGGCG GAGACGTGCT GTGCAGGGCT GGGGAGAACG AGGCAAGAGG CCAGGATCTG 1020 AGGCTTAGCA AGCGGACCGC TCTGTGGACC AGTGGCCCTC TGCCATTCCC ACTCTCTCTG 1080 CCTGGCCACT CCTCAAGGGT CTGGCTTCTT TGCTGCTGCT CACAGTAGAT GCAGTCTGGA 1140 AGGGTGCCTG GGGGACCCCA AACCCTCCAG CAGCCCAGGT TCTGATGTGG AGAAATGGTC 1200 ACCTCCTGTC GACCTCAGGC CCTCTGCACC TCTGACTGCA TGTCTCCCTC TGTCTCCTCT 1260 ACTTGATGAC GCTGCCTTCC AGCAATTTGC TGGCAAGCGG GCGGCCCTCT TGCCTTCCTA 1320 CGTGTCTGCG TAGTCTTTAT CCTTACTGCC CCAGACCTCT CATTCCCCAG AAGGGTGATG 1380 GCTGAGGAGG TATATCCTCT GCCAAAGATT CTGTTCCAGC TAGCCCATCC CTCTGCCCCC 1440 AGGCACAACC AGCAAGGGCC ACATCTAACC AGATGGTTGT CCTTTCTCCT CCAGACCTCA 1500 GAGGAAGGAG GCTCCCGATC TCCCTGGGCA ACCTGGATCC CTGACAAGAG GCTCTTTCAC 1560 TTTCTAAGCT TGATCTCCGG TGATGACACA CCCTGCAGGG CAGCAGCTGT GACTAATTCT 1620 GTGTTTTAGA CTCTGCCTTG TGCCTGGCTG GTGCCTGGGA TGCAAAGCTG CCAGTGAGAA 1680 AGGCACCCTG GAAGGGTGCA GGGAGGCTCC AGCTGCAGAG CTTTCCCAGG ATAGTGAGGG 1740 GGTGGGGCTG GAATGGCCCC AGAGAAGGTG GCCCCAAAGG CCAGGGCCCA CCCAGCATGC 1800 CTCAGTGCTG TAGGATCAGG TCTCAGCAGC CAGCTGGGAA AGCCACAGCC TGGCACAGGG 1860 AAAGGCAAAG GCCTTGAGGT GAGAGAGACC TCAGGTTTGA ATCCTGGCCT CGCCACTTAT 1920 CAGCCAGGTA CCCCGCGGCC TCCTGTACTC ACTTGTGAAA CGGAGGTAAT GATAGCACCA 1980 AACTTGCTGA AGTTCTTTGG GCCTAGAAGT AGGTAGAAAT GGGCTTTAAA AGAAGGGCGT 2040 ATGTTATCTG ACTTTGTCCT ACCGGATAGA ATTACTTAGC CCCATTTTAC AGGTGAGGAG 2100 CCTAAGGCAT GGAAGGGCCC TCTGAGCCCA GGCCTCTGCC CCAAAGCCTG TACTGTTTCT 2160 TGATGCACCA GGCTCACTGC AGGAGTAGAT GAAAGGAGGT TAGAGGCTTC TCATTCCCTG 2220 CAAGGCTGCC CGCTCACCAC TCTGAGTTCC TGCTGCTTCT GCCCCTCCCT CCTCCCACTG 2280 TCTCTTCTCC CAAACCAGAG CAGAGAGCTC TGGGGAGAAG GCCCCTTACG GAAAGATGTG 2340 AAGTCCCCAC CAAACACTGC AGAAGCAGCA GGTGGCTTAG CAGGGAATGC CACAGTGAGC 2400 TCCACACAAA AGAGATGAAC ACACGTCCCT TCCCTTTGTC GCCATGGATG TGGTCACACA 2460 TAGCCCCTAA TTGAAGGAAT CAGGGTACCT 2490
|