| Tag | Content |
|---|
EnhancerAtlas ID | HS060-16592 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr19:2411370-2413690 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr19:2413231-2413248 | AGGGTCAGGGTGAACTG | + | 6.11 | | NKX2-3 | MA0672.1 | chr19:2411645-2411655 | TTCAAGTGGT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr19:2412975-2412990 | AAGGTCAGGAGTTCA | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACCTGGAACC TTCTTTTTCT TCTTCTTCTT TTTTTTTTTT TTTGAGATGG AGTCTCACTC 60
TGTCACCCAG GCTGGAGTGC AGTGGTGTGA TCTCAGCTCA CTGCAACCTC CGCCTCCCAG 120
GTTCAAGCGA GTCTCCTGCC TCAGCCTCCA GAGTAGCTGT GATTATAGGC ATGCGCCACC 180
ACACCTAGCT AATTTTTGTA TTTTTAATTA AGACACTGTC TCGCTCTGTC ACCCAGGCTG 240
GAGTGCAGTG GCACCATCTT GGCTCACCTC CCAGTTTCAA GTGGTTCTCA TGCCTCAGCC 300
TCCCGAGTAG CTGGAATAAC AGGTGCCCAC CACCACGCCT GGATAATTTT TATACTTTTA 360
GTAAAGACAG GGTTTCGCCA TGTTGGCCAG GCTGGTCTCG AAATCCTGGC TTCAGGTGAT 420
CTGCCCACCT TGTCCTCCCA AAGTGCTAGG ATTACAGGTG TGAGCCACCA GGCCCGGCCG 480
ACAATTATAA TTTTTGTTTT CAAGGTGTCT CATTCTTTCT TCTTTCAGCC ACCTGGTCTT 540
GTTTGCAGTG TCCTGTTCTT GTTTCGTGGA TACCATTTCT TTCTTTTTCT CTGAGGATCG 600
TAATTTAATC CGTTATGTTT CTTCTATATT CTATATTTGT GGTTAACTGT ATTTCAGGCA 660
AACGTAAGTT ATTCTGTTGT AACTGAGTGT CTTTATTTCA TGGAGATTGG AATCCCTCAA 720
CTGGTGCTTA AGAATGAAAA GCTGGGTGCA GTGGCTCACA CCTGTAATCC CAGTACTTTG 780
GGAGGCTGAG GCAGCCAGGT CGCTTGAGGC CAGGAGTTTG AGACCAGTTA GGGCAACATA 840
GCAAAACTTT TGTCTCTACA AAAACAAAAA CAAAAACAAA AATTAGCTGG GTTTGGTGGT 900
GCATGCCTGT AGTCCCAGCT ACTTGAGAGG CTGAGGTGGG AGGATTATTT GAGCCCAGGA 960
GGTGGAGGTT GCAGTAAGCC AAGATCACGC CACTGTACTC TAGCCTGAGT GACAGAGTGA 1020
GACGCCGTCT CAAACAAAAT TGAAAATTTA AAAATGTCGC TCAATTCTTG CCGTGATCTT 1080
ATATTTGCTA TTCACTTTCT CTTGGCGAGG GACATTAACA GTTTGTGTTC TTGGATTCTA 1140
TGTACCCTTT CAAGGGACCA AAGACCTCCT GGTCTCATTT ATCCTTTGTG GTTGCCCAAA 1200
TCCCTTTTCT ACCCCAACCA ACCCAGGTCC TCTTGAGAAA GCTTTCTCTT GTGTCTTGAG 1260
CTTCTGCACA TGGGCTGGGC TGCCACTTCC TCTGTCAGCC TCTCGTGAGT CTTCATGGTT 1320
TCTGGTCCAC AACCAGGGAT CTCTCCTGCC TAATTTTTTT AGCATGGCTG TGGATTCCTG 1380
TCTTTCTTGT GCATACCTTT GCTCTTGTTT CTAAGGCCTG GTGGGTGAGG AAAAGATGGG 1440
AGAGACTGCT ACATGTGCTT AGATTGCCAT ATTGAAACCA GAATCTGGAG AAAATGCTAG 1500
GAACTAATGA GAGGGCTCAT GTTTAAGAAT GTAAGAGTCG GCCAGGCACG GTGGCTCACG 1560
CCTGTCATCC CAGCACTTTG GGAGGCTGAG GTGGGCAGAT CACTTAAGGT CAGGAGTTCA 1620
AGACCAGCCT GGCCAACATG GTGAAACCCC GTCTCTACTA AAAATACAAG AAATTAGCCG 1680
GGCGTGGTGA TGCGTGCCTA TAATCACAGC TACTTGGGAG GCTGAGGCAG GAGAATTGCT 1740
TGAACCTGGG AGGAGGAGGT TGCAGTGAGC CGAGATCACG CCATTGCACT CCAGCCTGGG 1800
CAACAGAGCA AAACTCTATC TCAAAAACAA AAACAAACAA AAAAACGATA CACAGAACGT 1860
AAGGGTCAGG GTGAACTGGA TATGGGAAGG TAAAAAATGG TGAGGCCGGA CGAGTGACAG 1920
CAGATGAGCA CTTTGGGAGC AATGCTGCAG CTACCAGTGA GATATATGGA GGCACCCGCG 1980
TGGCAGCCAT ACTGCCAGCC TAAGCAAGTG GTGACATTAT CAAAGATCTA CTGAGTTAAG 2040
AAGAGGAGGG GATGTTATTT ATTTGGGTCA CGTTTTGGCC TGCCAGAGGT AGGACTGAAA 2100
GACATCTTAG AGATCCTATA GTCCAACTGT CTTGGGTTTT GTTTTTTTTC CTCCACAGAA 2160
GAGGAAACAG GTTCTGAGAT GTCAATGATC AGCCCCAGGT GCTCTGTGAG CTTGTGTGGA 2220
GAGAGGTCCT GGCTGTCCCA GCTCAGAGCT CCTTCTTGGG CCTCGTAGCA CTGGTGTCTG 2280
GACTGGCTGC TGCCGACCCA TCCTGAGGGT GTGTGTTGGT 2320
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