| Tag | Content |
|---|
EnhancerAtlas ID | HS007-04222 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr12:119446280-119447560 |
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 | TATCTAATGT TGTGTAACAC CTAACCATGT TGGAGCTACT CTTATCTAAT GTTGTGTAAC 60
ACCTAACCAT GTTGGAGCTC TAAAGGTAGT AGTAGCCCCA GTCCTTGGCA AGTCTCCTCA 120
CCATGCCTCA GTTTACCCAT CTGTGAAAGT AGGCTACTGC CTTTGACTAT TTCTGAAGGT 180
GATTCTTTTC CTCACCTCCA GCTCCCGGTG AGAACGCATG TTTATCTCCT GATGGGCACA 240
GGTCTGCCCT TGAAACCCCT CCCTCATCAG TGCTGTTTTT CCCCTCCCCC ACCAGCCAGA 300
GCCAACGGGC CGCCCCTTCC TCCACCAGCT CTCCGGCCTT TGACACTAAT TGATACGGAG 360
TTTCCCCCTC TAATCCTGCC TCTGCCTGGG GCCCTTGTTC CTAGGGCATC TGCTTGGTGA 420
GAGGAGGAGG AGGCAGGGCC GACCGCCACC CGCCTGTCTG CCATCTGGTC CCCTTCCCCT 480
CCCTCCTCTC ATTGCCACCG AGGGAAATCT GTAATGAATC CGTGGCCCCC AGCCCAAAGG 540
GGTGGGGTAA GACCGGTCAC ACGCTGGCGG TCTACACACA CGCTCACACA CATACTCACA 600
TACACACACT CGCTCGCACA CGCAGCTTGT AGACACAATC ATTAGCAAAG CTTTTGTGCG 660
GCCCTCCCAG GCCCGCTGCA GCTGAACAGC TGCTGGGAGG GCTCCGGAGC GAGATGCTAA 720
CAGGAGGGGA ACTTTAATTA TCCCACCGAA TGGCATCTTG GGCAGACCCC GGGGACTGGA 780
CGAGATCGGG AAGAGGGAGG AGAGTAGGGG AGAGAAAGAC AATTAAAGTA GAGAATCCGG 840
GCCAAGAAAG GGATGGGACG CACAAGCCGA TGGGGAAGAG ATGGTAGAGG TTCACCTCTG 900
CTCCCTGTCT CAGAGGGCCA GATCTCTCCC ACTCAGGGGC TGAAGACAAG ACTTGGGAAA 960
ACGACCACTT TCTTCTCCTT TTCTGACTGG GGTTACCCAC ATGACTTTCT CTGCCTCAGC 1020
CATCAGAGTT GCCTTCTAAA AGCTTGGCAT CAAGAGCAAG GCTTTGATCT CTGCACATCT 1080
GGGTCTAATT TAGTTTTGCT TCTTGCCAGC TGTGTGACCT TGGGCCAACT ACTTCACCTC 1140
TCTGAGGCTT GGAGTTCTTC TGTGCAAAAT GGAAATCACA GCAATACCTA CTCACCGGGT 1200
TGCCAAATCA GTTAATATCA TTCATTCAAA CAGCAAATGT CCACTGAGTG CCTGCTGTAT 1260
ACAGGCACTG TGCTAGGAGT 1280
|
