| Tag | Content |
|---|
EnhancerAtlas ID | HS141-00139 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:11024900-11026410 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:11025700-11025715 | GAGGTCAGAAGCTCA | + | 6.15 | | RARA | MA0729.1 | chr1:11025700-11025718 | GAGGTCAGAAGCTCAAGA | + | 6.01 | | SPIB | MA0081.2 | chr1:11025389-11025401 | AAAGGGGAAGTG | + | 6.07 | | ZNF263 | MA0528.1 | chr1:11025271-11025292 | AGAGGAAGAGAAAGAGGAGGA | + | 7.36 |
|
| | 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 |
| GH01I010964 | chr1 | 11024590 | 11026962 |
|
Enhancer Sequence | TGGTGTTGAA CTCCTGGCCT CAAGTGATCC GCTCATCTTG GCCTCCCAAA GTGCTGGGAT 60
TACAGGCGTG AGCCACCAAG CCCAGCCAAG GCTGGGTTTA TGAGACATAA AATTCCCATT 120
TTACAGATGA GGCAGTTGAG GCTTAGAGAA GGTAAATGAC TAAGCCAAAG GCATGTGGCC 180
ATTTCTGAGA CTAGATGTGA GAGCTGGTCT AGCTCATTCC GGTACAAGGC GGACTTCAAA 240
GATGTCAAAC CAATGGGTCC CTCTGCCCCT CCCAGGCTGC CCTCATTCAG CCACATAAGA 300
AGAACCCAAG TCTAAGCTTT GCGGTGGGGC CTGAGAAGGG TGACGGGGCT GTCAGAGAAG 360
GGCGACCACA GAGAGGAAGA GAAAGAGGAG GAGCAGGGTA GTTCCCAAAA TTCCTTCCCC 420
CACTCCAGAC CACAGCCCCA CTCAGGAAAA ACTCTGGACT GGGTCAAGGA AGGGAGCACA 480
AAGAAATGGA AAGGGGAAGT GGAGGTGAGG AAAAGACAAG AAAAAAAAAA CTGTGAGCCA 540
AACTGTGCGG CTGGTTGTCC CCTTGCAGGA CCCCTGGAGT GAAATTTAAG TAACAAGAAT 600
GCTGGCACAG TGGCTCATTC CTATCATCTC AACACATTGG GACACCGAGG CGGGAGGATG 660
GCTTGAGCCT GGGAATTCCA GACCAGCCTG GGCAACATGG TGAAACCCCA TCTTCTACAA 720
AAAGTACAAA AATTACCTGG GTGTAGTGGT GCATGCCTGT AGTCCCAGCT ACTCTGGGGG 780
CCGAGGTGGG TGGATCACTT GAGGTCAGAA GCTCAAGACC AGCCTGGCCA ACAAGGTGAA 840
ACCCCGCCTT TACCAAGTAG TCTCAGCTAC TTCAGAGGCT GAGGCAGGGG AATCGCTTGA 900
ACCTGGGAGG CGGAAGTTGC AGTGAGCCGA GATTGCGTCA CTGCACTCCA GCCTGGGTGC 960
CAGAGCGAGC CTCCGTCAAA AAAAAAAAAA AAAGGAAAAA GAATACAAAA ATATCTTGCT 1020
TCTGTAAATT TTAGAGTCAC ATGGTCTCGT GAGCCCATAA TGGGCCTGTG CAAGTGAGGG 1080
CTGTCAGTCA GTCTTTGCAA CTCCTCAGCA CCATTTATTC ACTTCATTCA GCACTTACTG 1140
AGTACCTACT GTGTGCCAGG CCCTGAGGCA AGCCTGTGGG TGTGACTGCC TCACCCCAGA 1200
GACTCCAGGT CCAGCAGGAT ATGGTGTGTG AGTGGGCACA TTATGAGTCA GTGTTGGCAA 1260
TGATAGAAGC AGGTCTACTG CACAGAGAAG GGGGGATTCT CAGGAGGACT GCCTGGAGGA 1320
GGCAGCATCT GAGCTGGGCG GCCTTTTAAT ATCTATGCCC ATAAACTCCA TGAGGGCAGA 1380
GACTTCTGGT CTCCCTCAGC TCAGTTTCTG CAGAGGAATA ATGGTGCAGT GTCTCCTTAC 1440
TTGATATCTG AGCTCAGGCT TAGCTCCTTA AATCTCCCTT TAAAAAAAAA AAAAGAAAAG 1500
TTTCCCAAAC 1510
|
