| Tag | Content |
|---|
EnhancerAtlas ID | HS141-04168 | Organism | Homo sapiens | Tissue/cell | NB4 | Coordinate | chr12:27590560-27591450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr12:27591227-27591238 | TTCTGTGGTTT | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 27590616 | 27591000 | | chr12 | 27591000 | 27591085 |
| Enhancer Sequence | TACAACTGGC ATGAACAGTT CACAAAGGGA AGGGGGTTCT TCAGGGGAAA GAATCTATGC 60
ACAGAGCTCT CCTGCCATAA ATCAGTTTCC TTTTCCTAAA CTACCAGTTC ACCTGCATGC 120
GCAGCTCCAG CCTACTTCCT GTCAATATGG AAGAGAGCTC CTTTTGTCCA AAGACCCCTT 180
CACCTGGGCT CTGTATCTGA TTTCCCCTCA ACACCTCAGT CTGTCTCCCT CTTTTGTATC 240
TTCAACATCT CCCTCTTTTC TAAATCCTTC CCTTGTGCAT TTAAACCTGC TCTGTTTACT 300
CTGATCACAA ACACAATCAT CCTTAGGCCC CATGTCTTTC TCCAGTGACC ACCCTCCTCT 360
TCACAGTTGG GTTTTTATAA GACTTGCCTA CACTCCCGGG CTTCCTGCTT TCACTTCTCC 420
AATTCACTTC TTGTCTCACC TCCTCCACTG AAATGCTTCT CTTCAAGGTC ACCACTGACC 480
TCTTGGTGTT CTTTAACATT TATTTCTCTG GAATGTTAGT CACTGCAGAC CACTTCTTCC 540
CTTTCTTGAA TCTTCCTCCC TCAGCTTCTG TGATATCTCA CTCCTGGTTT TCCTTTAACC 600
CGCTGGCCAT TCAAATGTCA GAGTTCCTTT AGGCTTCATC CTAGGGCTGC TTTCTACTTG 660
CTTTATTTTC TGTGGTTTCA TCCACTCCTA TAGCTTTACT ACCATTAATT GATGATAACT 720
CTCAAACCTA TGATTCCATC CTGATCTTCT CCTTAGCTCC AGAGCAATGC AGCCGACAGC 780
CTACTGGTCA TATCTGTTAA TATGTTCCAG GGAGAACTTA ACCTCAACCT GTCCAAAGTG 840
CAATTCATCA CTTTGCCTTT CTTCCCTAAC CTGCTTTTCC TCTATTGTCC 890
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