| Tag | Content |
|---|
EnhancerAtlas ID | HS003-48127 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chrX:9347080-9349190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chrX:9348147-9348161 | GGGGAATGAGTCAT | + | 6.2 | | Myod1 | MA0499.1 | chrX:9347508-9347521 | AGAAACAGCTGCA | - | 6.29 | | Myog | MA0500.1 | chrX:9347511-9347522 | AACAGCTGCAG | + | 6.02 | | TBX20 | MA0689.1 | chrX:9349060-9349071 | CTTCACACCTT | - | 6.32 | | TBX21 | MA0690.1 | chrX:9349061-9349071 | TTCACACCTT | - | 6.02 | | Tcf12 | MA0521.1 | chrX:9347511-9347522 | AACAGCTGCAG | + | 6.62 |
|
| | 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 |
| GH0XI009378 | chrX | 9346986 | 9348664 |
|
Enhancer Sequence | TACAGTATAC TACAGTACAG CGTAGTACTG TGTAACGTAC ACTGTCAAAC CACATCATTT 60
GGGTTCACAT CCAAGCCACT CATTTACTCT GCAGCCTAAA GCAAATTGCT CAATCCTTTT 120
GTGTGCCCCA GTTTCAACAT ATTTAAAATG TAGTAGATTA GATCATTGTT AGGCAAGTAC 180
TCATTCCTGA CACCACTTCC TCCCAACCTT CGTGGAAGGA GTATACTTAC CCACTCCATC 240
CGTGTTGGCT TGACACTATA AGTTGCTTCG AACTCATGCT GGGCAGAGTG TACATCCCCA 300
TCTCTTTATT TGAGGCTCAG CAATGTGCCT CACTATGGCC AATATGAGAA GATGAGACAC 360
AAGTGGAAGC TTGAAACGAA TTGTGCAGTT TTGCTTTCCC TCTTGAACGT CTCCCATGAC 420
TATGGGAAAG AAACAGCTGC AGTTTGCCTG CTAGTTTAAG GAGAAAGATG CCTGGAGCAA 480
ACCTGAATCC AGTGTGCAGC TTGGAGCTAT GTGCAGATAA GCTCAGACTA AATCTTGCTG 540
GCTCTCAGCC AAGCTGTGGC CACATTGGGG AGATTAAATG ATTGCTGTGT TCAGCCATAG 600
AAATTGTTTG GGGATGCTTC TTATATGGCA TTATTGAGGT GCTAGCTGAC TGACAGAGAT 660
ATCAATGATA GAACCTATTT CATAGGGTTG TGAGGATTGC ATGAGATAAT GTATGTAGCA 720
CATTTAAAGC ACTGTCTGGT GCTGGAGCTT GTTCACAGAG CCTTTGAACT TCCTCTCGGA 780
ATATGCAGTT GCCCCTCCAG CCTCCTCTGC AGGGCTGCTT TCCCTGGCCC ACGCACTCCA 840
CAATGTTCCA GACTTCCTTG TCCTTCACTG TACTCAGCTT CATCCTCTCA TGCCTTTCCA 900
CACCTTTCCA GGTGTTAAGT AGCTGATCTA ATTCATCCAT GTTAGCACAA TAGTGGGAAA 960
ATGCTACCTC CACCTTACCG CCTCCGCCCT TCCTGGAAAC AAGTGGTTTG TTATTTTTGT 1020
TTGTTTTAAA CATTTATTGG AGTCAAAGGC TCCTTTTGTC TCATCCTGGG GAATGAGTCA 1080
TGATGAACAA CTCAGACAAG GGATGAGGGG ATGGGCAGGC TGTTACAAGC TGGGTAGCAG 1140
AGGAAGGCTT CTGTGAACGG GAGAACAATT TCTCTGAAAA ACCAGGTAGA GCTTTGAGGC 1200
AACCCAGACC TTCAGAGCAT GCAGGGCTCA TTCAAATCAC CCACAGCCCA GCTCTCCACC 1260
TGTGCTCAGG GCCAACCCCG TCACTCCCCG CGCATGCAGG TGGCCATTGT TGAGAGCACT 1320
AACTGATACC CCAAACCTCA CCCGAGGAGC CACAGGAAAA CTCTTATAAA GGGGTCAAGG 1380
GAATGGAAGA TGCTGCACTG GCCTGAGCTA CAGGAACCTC CAACCTCGTG ACCAGAGGAG 1440
GCAGCAGGGG TGGGACCCCT CAGGTATGGC TTGCATGGAG ACCAGCCAGG ACAGGATTTC 1500
TCACCCTTGG CACTGCAGAC ACTGGGGGCC AGCTTACTAT TTGCTGTGAG GGCTGTCCTG 1560
CGCATGTAGG ATGTTAAGCA GCATCCTTGA CTCCATCCTC TATATGCCAG TAGTACCTCC 1620
CCTACTCCCC ACAGCTGTGA CAATCAGCGA TGTCTACAGA TATTGTCGAG TATTCTCTGA 1680
GGGACGAGGG TCAAAATACC CTCAGTTGAG AACCGCTGAG CTAGAGGCAT GGAGCCAGAA 1740
CTGAGATCAC AACTATTCTG TCAACAAACA CTTCCTAAGC ACCTATCATT TGCTAAGCCC 1800
TGTGCTAGAA TCTGAGAGTA CAGGGATACT AAGGGGGAAA GACCTGTAAA TAATGAATAG 1860
TAATATCACG TGGTTACTCT CCCATAATCA AGTGGGAGGC AGGCAAGGAT TCAATCTGCT 1920
TGGGACAGAA AGAGTCAGGA ACCACAGCCA GAGTGGGCAC AGACGCCCTA ACATGCTTCC 1980
CTTCACACCT TCCTCTGGCA GCACTGCACA CTGGGGAATG CCTGCTCCCT CCTCCTCCTC 2040
TACAGCAATT TATGCATAAT CAGAGCCCCT CACTTCAGAA GATCCCAGAT ATACGGTCAA 2100
GTAATCCTGT 2110
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