| Tag | Content |
|---|
EnhancerAtlas ID | HS078-05431 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr14:65604170-65605370 | 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 | AGCTGGGATT ACAGGTGTGA GCCACTGCGC CCGGCCAATT TTTTTGTATT TTTAAGAGAG 60
ACAGGATTTC CCCATGTTGG TCAGGCTGGT CTCGAACTCC TGACCTCATG ATCCGCCTGC 120
CTCAGCCTCC CAAAGTGCTG GGATTACAGG CATGAGCCTG GCCTAGTGAA CCATCTTCTT 180
ATCAGCCAGT CGGATTCATT ATCAGCTCCC AGGCTTCTAG CAACTACGAA TGATCAATGC 240
ATTGGACTGG AGCCACTACC CCAGGGGAAA AATGGCCACT TCCAGCTTAT GTGGGATCCA 300
GCCAAATGCC TTGTGGAATG GAGATGTAGG AGTATTGTTA GTCATGTCTG GGCCTGCCAG 360
ACTAATTTTC ATCTTCATCC AGTTTTCACT CTCTGGAGAG GGGAGCCCAA GCAAAACATC 420
TGCGATACCA CCGCCCTTCC CCGTGGCCCA TCCCCACTCA CTGAGCTGTT TAAGATTCTC 480
CTGCTGTTCT GTGAAGAAAA CAAGAAGCTC AGGTGCTGTT CCACCAGGCA ATCCCCATCC 540
GCCCTGCACG GAGTTTCGGA CTTTTCCTAG ATTATTCCAC AAGCCTCCTT AACAAAGTGG 600
ACCAGTGTTT ATCCTGCACC TTTGTTTTAC AGACTGTTTT ATGACTGGAA ATAACCTGCT 660
TATCATGAAT CTCTCCCAAG GGATTTATCG AGGCATCGTC TATTCCATTT TCCTGGCTCT 720
TTCACACATT TATTTCACTT TCTTCATTAT TTGGTGAGCA CATTTTGTAT TCCAAGTCTT 780
AATTATACAA GAAAGAAATA TTGTCCAACA AACACAGCCC TTACTGGATT GATTCAGTTT 840
TTTTTTTTTT TATTTAAAAG GTAGGCTTGT CCCCCTTGGT AGTTCTCTGG CTTTTAAAAT 900
ACGTTTTCTC TATGAAATCC TAGGAAAGGC CCATGATAGT GGTGTCTTTG TGCCTGTGGG 960
CTTCCAAGGG TGCAAAATGC TTTCTTCAAG GAATAAGCTC AAGTTTATTA TTGACCATGT 1020
TTTACAAACT ATCTTTTTTG CAAGGAATGG ACAAAAGTCC ATTCTAGCTT TTGTTTTTCT 1080
CAATCACTAA TGCCTAGTTT GGTCCTTGAC TTCCAAAGCT CTCTTTAACC TCTTGGGATT 1140
GAGGGGAACT TTCAGCCTGT CTTCTGGCAT TTTGTATGTG TGGAAGGGAT AAAATATACT 1200
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