| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06619 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr12:7146210-7147620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:7147168-7147186 | CTTTCTTTCTTTCCTTTC | - | 6.03 | | IRF1 | MA0050.2 | chr12:7147176-7147197 | CTTTCCTTTCTTTTTCTTTCT | + | 6.09 | | IRF1 | MA0050.2 | chr12:7147180-7147201 | CCTTTCTTTTTCTTTCTTTTT | + | 6.18 | | IRF1 | MA0050.2 | chr12:7147186-7147207 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | | TP63 | MA0525.2 | chr12:7146918-7146936 | GACTTGTTCTTACATGTT | - | 6.59 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTAGAGTTG CTGGTCAGGA ACTGGAGAGA GGCCTGGCGG GCCTGGTTGT GTTTGTATTT 60
GGGCTTTCTC TGGGGCCGTG GAGTGATAGG AAAGGTTGGC GTTTCCCTTG GAGATGCACC 120
TTTTCTAGTG ATTGTGTTTG CAGGGTGAGT CTGACCCGCT GAGCCACAAT GAGCAAGGAC 180
AAGGAATATT TTTCAATTAA CTTCTTAATT CTCGTGAGTG TGGCTTATGA TCTCCTTTGT 240
GGTTTGTTGA TTATAAGGCG CACCCTGACG TTAGAAATAA TAAAATGAGT GTGCCTTAGC 300
ATCAGAGTGT CACCATCTGA CGCTCTAGGA CTGGGCAGAG CCCAGGTCCT CTTCTCTGGA 360
GTACTCGGCT ACCACCTTGC CGTGCAGGGG GCTCCCTCCC TCCCTTCACT GCACACTCTC 420
GGTTACTTCT TTCTCAATTC CATCCGCACA GCTTCCTGCC TCAACCTTTT CTGCCTTCTG 480
CAGGAGCAGA TGTTCCCACA AGGAACACGG GAGGTGCCAA GGTTGGGTTT CCAGCATAAG 540
GCTGAGCCTT CTGCCCTCGG TTTGACCCTG GGTGGCACTG TTAGCTGGAG GCCACGAGAG 600
CTGCCTTGGA CGTGTGGGGC CAGCGAGCAG CGGCCCCTCA CTCGTGGAGC ATTGTTGCAG 660
CCGGGCAAGT CTGCCATTGC TCATCCTCTT AGTCTTGCTC CCAGCTGCGA CTTGTTCTTA 720
CATGTTCTAG ATGCAAGGCT TTTGTGTGTG TGTGGTTTGT AAATATTTTG TCCCAGTCCA 780
TCGCTTATCT TTTACATCCT CTTAAGGGGG GTTTTGCAGA GAAAAGGTTT TTTTCTTTTC 840
AAATTTGGTG AAGTCTGATT TATCAATTTT CCTTTTTAAG GATCTGATTT TGGTGTCATG 900
GTTAAGAATT CCTCAATGAC TCCCAGGTCC CAAAGATTTT TCCTACCTTT TCTTTGCTCT 960
TTCTTTCTTT CCTTTCTTTT TCTTTCTTTT TTTTTTTAGA TGGAGTCTTG CTCTTGTTGC 1020
CCAGGCTGGA GTGCAATGGC GTGATCTTGA CTCCCTGCAA TCTCTGCCTC CCTGGTTCAA 1080
GCAATTCTGC CTCAGGCTCC GGAGTAGCTG AGATTACAGG TGTGCACCAC CACACCCGGC 1140
CCAGGCTGCA GTGCAGTGGC ACGATCTCGG CTCACTGCAA GCCCTGCCTC CCAGGTTCAC 1200
GCCATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGCGCCCGC CACCACACCC 1260
GGCTAATTTT TTTGTATTTT TAGTAGAGAC AGGGTTTCAC CGTGTTAGCC AGGATGGTCT 1320
TGATCTCCTG ACCTCGTGAT CTGCCTGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCG 1380
TTGAGCCACC GCACCTGGCT TCTCTGTTTG 1410
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