| Tag | Content |
|---|
EnhancerAtlas ID | HS038-05256 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr12:119446400-119447620 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr12:119447451-119447463 | GAAATCACAGCA | + | 6.22 | | Gfi1b | MA0483.1 | chr12:119447452-119447463 | AAATCACAGCA | + | 6.62 | | Tcf12 | MA0521.1 | chr12:119446964-119446975 | AACAGCTGCTG | + | 6.32 | | ZNF263 | MA0528.1 | chr12:119447068-119447089 | GGAAGAGGGAGGAGAGTAGGG | + | 6.08 | | ZNF263 | MA0528.1 | chr12:119447075-119447096 | GGAGGAGAGTAGGGGAGAGAA | + | 6.32 | | ZNF263 | MA0528.1 | chr12:119447072-119447093 | GAGGGAGGAGAGTAGGGGAGA | + | 6.36 | | ZNF263 | MA0528.1 | chr12:119446748-119446769 | TCCCCTTCCCCTCCCTCCTCT | - | 8.58 |
|
| | 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 |
| GH12I119008 | chr12 | 119446337 | 119447506 |
|
Enhancer Sequence | CCATGCCTCA GTTTACCCAT CTGTGAAAGT AGGCTACTGC CTTTGACTAT TTCTGAAGGT 60
GATTCTTTTC CTCACCTCCA GCTCCCGGTG AGAACGCATG TTTATCTCCT GATGGGCACA 120
GGTCTGCCCT TGAAACCCCT CCCTCATCAG TGCTGTTTTT CCCCTCCCCC ACCAGCCAGA 180
GCCAACGGGC CGCCCCTTCC TCCACCAGCT CTCCGGCCTT TGACACTAAT TGATACGGAG 240
TTTCCCCCTC TAATCCTGCC TCTGCCTGGG GCCCTTGTTC CTAGGGCATC TGCTTGGTGA 300
GAGGAGGAGG AGGCAGGGCC GACCGCCACC CGCCTGTCTG CCATCTGGTC CCCTTCCCCT 360
CCCTCCTCTC ATTGCCACCG AGGGAAATCT GTAATGAATC CGTGGCCCCC AGCCCAAAGG 420
GGTGGGGTAA GACCGGTCAC ACGCTGGCGG TCTACACACA CGCTCACACA CATACTCACA 480
TACACACACT CGCTCGCACA CGCAGCTTGT AGACACAATC ATTAGCAAAG CTTTTGTGCG 540
GCCCTCCCAG GCCCGCTGCA GCTGAACAGC TGCTGGGAGG GCTCCGGAGC GAGATGCTAA 600
CAGGAGGGGA ACTTTAATTA TCCCACCGAA TGGCATCTTG GGCAGACCCC GGGGACTGGA 660
CGAGATCGGG AAGAGGGAGG AGAGTAGGGG AGAGAAAGAC AATTAAAGTA GAGAATCCGG 720
GCCAAGAAAG GGATGGGACG CACAAGCCGA TGGGGAAGAG ATGGTAGAGG TTCACCTCTG 780
CTCCCTGTCT CAGAGGGCCA GATCTCTCCC ACTCAGGGGC TGAAGACAAG ACTTGGGAAA 840
ACGACCACTT TCTTCTCCTT TTCTGACTGG GGTTACCCAC ATGACTTTCT CTGCCTCAGC 900
CATCAGAGTT GCCTTCTAAA AGCTTGGCAT CAAGAGCAAG GCTTTGATCT CTGCACATCT 960
GGGTCTAATT TAGTTTTGCT TCTTGCCAGC TGTGTGACCT TGGGCCAACT ACTTCACCTC 1020
TCTGAGGCTT GGAGTTCTTC TGTGCAAAAT GGAAATCACA GCAATACCTA CTCACCGGGT 1080
TGCCAAATCA GTTAATATCA TTCATTCAAA CAGCAAATGT CCACTGAGTG CCTGCTGTAT 1140
ACAGGCACTG TGCTAGGAGT CAGGGATACA AGAGAATGCA TGATGTGGGG TGGGAGTGCA 1200
GACAATAAAC AAGGGAACCA 1220
|
