| Tag | Content |
|---|
EnhancerAtlas ID | HS095-09140 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr14:65603970-65604950 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox3 | MA0514.1 | chr14:65604788-65604798 | CCTTTGTTTT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGATTCTCC TGCCTCAGCC TCCCGAGTAG CTAGGATTAC AGGCACGCGC CACCACACCT 60
GGCTAATTTT TTGTATTTTA CACTTTTTTT TGGTCTTTTT TTTTTTCTTT CTTTCTGTGG 120
AGAACGAGGT CTTGCTATAT TGCCCAGGCA GGTCTTGAAC TCCTGGGCTC AAGCTATCCT 180
CCTGCCTCTG CCTCCCTGAG AGCTGGGATT ACAGGTGTGA GCCACTGCGC CCGGCCAATT 240
TTTTTGTATT TTTAAGAGAG ACAGGATTTC CCCATGTTGG TCAGGCTGGT CTCGAACTCC 300
TGACCTCATG ATCCGCCTGC CTCAGCCTCC CAAAGTGCTG GGATTACAGG CATGAGCCTG 360
GCCTAGTGAA CCATCTTCTT ATCAGCCAGT CGGATTCATT ATCAGCTCCC AGGCTTCTAG 420
CAACTACGAA TGATCAATGC ATTGGACTGG AGCCACTACC CCAGGGGAAA AATGGCCACT 480
TCCAGCTTAT GTGGGATCCA GCCAAATGCC TTGTGGAATG GAGATGTAGG AGTATTGTTA 540
GTCATGTCTG GGCCTGCCAG ACTAATTTTC ATCTTCATCC AGTTTTCACT CTCTGGAGAG 600
GGGAGCCCAA GCAAAACATC TGCGATACCA CCGCCCTTCC CCGTGGCCCA TCCCCACTCA 660
CTGAGCTGTT TAAGATTCTC CTGCTGTTCT GTGAAGAAAA CAAGAAGCTC AGGTGCTGTT 720
CCACCAGGCA ATCCCCATCC GCCCTGCACG GAGTTTCGGA CTTTTCCTAG ATTATTCCAC 780
AAGCCTCCTT AACAAAGTGG ACCAGTGTTT ATCCTGCACC TTTGTTTTAC AGACTGTTTT 840
ATGACTGGAA ATAACCTGCT TATCATGAAT CTCTCCCAAG GGATTTATCG AGGCATCGTC 900
TATTCCATTT TCCTGGCTCT TTCACACATT TATTTCACTT TCTTCATTAT TTGGTGAGCA 960
CATTTTGTAT TCCAAGTCTT 980
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