| Tag | Content |
|---|
EnhancerAtlas ID | HS138-29161 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr3:194600130-194601550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox3 | MA0514.1 | chr3:194600715-194600725 | AAAACAAAGG | - | 6.02 | | ZNF263 | MA0528.1 | chr3:194600935-194600956 | GGAGGAGGAGAAGAGAGGATG | + | 6.47 | | ZNF263 | MA0528.1 | chr3:194600932-194600953 | GAGGGAGGAGGAGAAGAGAGG | + | 7.38 |
|
| | 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 |
| GH03I194878 | chr3 | 194599409 | 194602568 |
|
Enhancer Sequence | AAGAGGTGGG GTTGATAGGC ATGCACGGAC AGACTGATAA GCCTTTCGCA GGTTCACCAA 60
TGTTTCATGA GCTAAAAAAT ACTGTGATCT GCACAATTGT GTAGGTAGGT ACTATTATTA 120
TTCACAATTT ACAGATGACA AAAAGAGAGG AATCAAAAAG TTGAGCAAAC TGCCTAACTT 180
GCAACACAGT TATGAATAGA GGAGCTAGAA TCTGAAACCT GGCAGTTGGG GGCAGGGCCT 240
GCGTTAGTAA ACATGGCTTG TGCTTACACA CATCCATGCG CGTGCACACA CACACACACA 300
CACACACACA CGCACACGCG CGCACACACA CTTCCCTTTT CCATCCCAAA CGTACCACTC 360
AGAGTCTAGT TGAATTTTGT AGTTTCAATT CTGACTTTGT TTCTTTGAAG CCCAATTGCC 420
CTGATGCTGT TGACGGTTGA CCTCCAATGA GTGGGAGGGT CACAGACACC TTTATTTTCA 480
TTTCACAGTC TTCTGCATTA TTTTGATTTC TGCCCATGAG CATGCATTAT ATTTATAAAG 540
ATTAATTTTA AAACACATTG CCCCTCATGG GGAGGACTGT GTTTCAAAAC AAAGGTTTTA 600
AAGTTTAATG AACGTCTAAA AATCCTTTGC CATCACAGGT TTTCAGAGTC TTATTTATCA 660
AATGCCCTGG CTGCTGGGGA TCTTTCCAAC TCATGCTGGA ATCGGGCCTG GGTTTCCTGA 720
TTTCCCCAGC TCCAACGCTC AGCCTCAGCA GCCAAACCAG CCCGGCCCCT TCCTGTGGTT 780
TCCAGCTCAG CCCTTCTGGT GGGAGGGAGG AGGAGAAGAG AGGATGCCCG TGTTGGGCCC 840
TTCCCATGGG GCCCCAGTGT TTCGTGAAAA CAGGGTCATG TCAATCACAG TCCAGACCTC 900
TAAAACCTAG TAATGGAGGC TCAAGGCAGG TGAAAACATA CAGGGTGATC AGAATCAAGG 960
CAAGGAGGAC TCAGGAAAGG GGACGGCACT CAGGCCAGGA GAGGGCTAAG CCCACTGGGC 1020
AGAGTTCCTG CCAGTTGGAA CAGGATGGAC TCCTAAAGCT CTGGCCTGGC CTCACCAGTG 1080
CTGTCTTTTC TACTTTTCTT CTGGGGTCCA GGGGCATCCA AGAGCAAGAT TCCACCAGGG 1140
CAATGGACCC AGGAGGGGCT CAGGGGCCTG CCCCTGCCTG GCCTGAAACT TGGCACACAC 1200
TGGTCCCATC TGGCAGCCAG CTTTAATTAC GTTTCTGGAC AAACACACTC TCATGCATTG 1260
GGCATCAGAG TGGGGACACT GTCAGGCAGA AGGAGGAGAG AGAGGCAGGC TGGCTCACTC 1320
CTGTTATGTG TACCCACTTA GCAATGCCAC TTTAATTTCT CAAAGACATT CCCTGACAGC 1380
TCCATGCTGC GCCCGGCACA GGGAGCCTAG ACCTGCTAAT 1420
|
