| Tag | Content |
|---|
EnhancerAtlas ID | HS175-05414 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr12:1014490-1016130 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr12:1015270-1015281 | TTTGACCTTGA | - | 6.14 | | Esrra | MA0592.2 | chr12:1015271-1015282 | TTGACCTTGAA | - | 6.14 |
| | | 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 |
| GH12I000905 | chr12 | 1014397 | 1015630 |
| Enhancer Sequence | GAAGGTTTAG CTGTATGGTT GACTCTTCCT CATGGTTTCT CTTTCCTCAT AGAGAATCCT 60
GTATTAGGTA ATGTAGGGTA AAATGAAAAG TGAAATTTCG TTCTAAAGGG GCCTCGCAGC 120
ATCAGGGGCG ACAGACTAGA GAGGTGTGTC TCCCAGCATG AGCTCTGTGG ATAAGCAATG 180
GTCACGCCTC CTGAGCTTCT TGTATTTAGC TTTTGACAGC TCTGCTCCCC TGTGATTATT 240
TCTGTTTTTT GTTTTGATTG TCTCTCACAT CAAGCTCACC AAGCAATAAT TGTTCAAACA 300
GGATGACAAT CCCCATGCAT GTGATATGCT TGCTTTCTAG ATTGAGTCAC TCACTGTCAT 360
GACTGCCCAT CCTCATTGCC TGTGCTTCCC ACTTCACCAC TCTCTCACAT TGGCTGTTCA 420
TGGAAGGCTG TTTTCTGTGC TCTCATGCTT CTCCCCTCGC GTTTCCTGTA CTGTAGGGAG 480
CTTACTCTTC CCTTCACACT GTATGTGCAA TAGCAATCCC CTTGTGGCTC CAGCAGACAC 540
CAAGAAATGA GCTGACACTC ACACTGCAGT AGTTCCGTGT CTTGCCATAG CGGTAAGAAG 600
CATGTGACCT TCCTCACTGC AGCTTCACCT CAGAATTAGC TGTTACTGCA GCACAGACCT 660
GCTTGTGTGT GCCATTCCCC AGGTGGTAGG ATATAAGCTT GACTTGAGAC CAGCGATGGT 720
CAGTAACAGG CTTTGAAGTG GCAGGATTGC GTTAGGTGTG CTGCTGTGAT CTGGTGCTGC 780
TTTGACCTTG AAAGCAGGAT AACGCATGCA CTTACTTACC CCCGCATTAC TTGGGTACCT 840
TAAGGACTAG TGGTTCACAA CTTACTTTAG GAGCTTTTAT TTATTCTGTA ACACGTGAGA 900
TCTGGTAAGA CAGTGGGGGG TAAGGAAAAC AGACAAGACC ATGACTCTTC TTTCCCTCTT 960
CCCCAAAACG TGCCTCTTGG AATAATCTTC AGTGTGCCCT CCAGCAGAGC CGAAATCAGG 1020
CAGGCATAGA CTCCCTCCTC TCTCATCAAA CCGCAGAAAT AGAGTTCCTT CATCATAACC 1080
GCAAAGCTTC CTCCTCCCCT TTGCACCCTG CCTCAGCTGC ATTTTCTTGT CGCTTCTACA 1140
TGGGAGTGCT TGCTGTTCTG GGAAGAGTGG GGAGAAGCGG TGGGAATCCT TGAGCCAATT 1200
GAAACTGAGG TCATCTTCAG GAAAACCATG TCTTCCTGAA GTTGAAAGAT TCAGGCACAC 1260
CATACAGTCC TTTCCTCATG AATAATCTTG TTCTTTACTC ATGGGAAATT GGGAGAGGTT 1320
AACCCCTCCC AAGTTTATGT TTGCAAATTC ATGTTTATGG GTCCAGGTGA AAAACTTTTC 1380
TGAACACAGC ATGCTACTTC TCTTATTACC TCTCTCTATT TAAAGAATGG CTAGGCTGAG 1440
CATGGTGGCT CACACCTGTA ATCCCAGCAC TTTGGGAGGC TGACATGGCA GGATTGCCTG 1500
AGCCCAGCAG TTCATGACTA AGCAACATAT GGAGATTCTG TCTATATAAA AAAGTAAAAA 1560
ATTAACTGGG TGTGGAAGTG CATACGTCTA GTCCCAAGCT ACTTGGGAGG CTGAGGCAGG 1620
AGGAGTTGGA GGCTGCAGTG 1640
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