| Tag | Content |
|---|
EnhancerAtlas ID | HS128-01837 | Organism | Homo sapiens | Tissue/cell | MCF-7 | Coordinate | chr1:207018930-207021570 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr1:207021446-207021459 | GAACATCTGGAAA | - | 6.32 |
| | | 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 |
| GH01I206847 | chr1 | 207020496 | 207021580 |
| Enhancer Sequence | TGCTTAAGAA ATACATGCTA AGAAGCCAAG AGTAACATTA TCTCCCAAAC CATGCTGAGT 60
CCTCTGTCAG CCCCTAGTAG GTACCCTTGA AAAATCTGGA GCTCACCTCC ACTGCTAAGG 120
TGCAAGGGGA GGGAATCCAT GTCACGCACC AGGGCCATGA CAGGTACTTT ACACATAGGA 180
CCTCATTCAA GCCTCAGAGG AAGCCAAGGG GGTTGGAGTT CTTATCCTCA CACGGTCAGT 240
GAAGGCATCT CAGGCTCAGG GAGGTGGGGG AGCTTGCCCA AGTCCACAAA GCTTTGGGAT 300
GGCAGATCCA GAAAATGAAT CCAGGCCCCA TCTTCCTGGC TTTGGTGCCC TCTCCTTTTG 360
CTGCTAGGGG AGTTCCTTTT ATCCTGGACA AGACTGTATA ACCTAGGGCC CAGGTTACTA 420
TGTTGAATGC CAGCAATGAA GATAACTAAA CCCAGATGCA CCAAAAGGGG CTTGGACTAA 480
CTAGCCACAA GCTTCTGAAG TTACACATGA AATTATGGAC ATACACAGAG CAAAGGAGCA 540
GAGGCCAACT TCTGAGTATG TCACGCAATG TTCCCGGCCC AGCTGAGGCC TGGGCTCCTC 600
CTGGGGATGC TCTATCCTCC TTCCATCTTC CAGAGCAAAT TGTTAATAGC CACACATGTT 660
CATACTGCTG AAACTTCATA CTGCTGAAAA AGGCACTGAA GAGGTAGGAA AAACAGTCTT 720
GAATCGCTGA TGCCACCCTG TCCCCAATCC CCCATCAGTG GCAGTGTGGT GCAGAGAGCA 780
GTTTTGTGTT CTGGGGAGAG GGAGAGCGCA GCAATTGTGA GGCATTGAAA TCAGTACTGT 840
CCTTGTTACA GGAGAAAGCA AAACTGGAAC ACATTCACCT GATGGCCACC CATGGAGGGA 900
GATTTAAACC AGCCCTACCC AGAGGGGAGT CACTGACCCC AACAGTCAGA ACTTGAGTTT 960
CTGCAAGCCT TACCACTGTG GGCTAAAGTG CTCTGGGGTT CCAAATAAAC TTGAAATTCA 1020
GTCTAGGCCA GAAGGACTGC AACTCCTAGG CAAGTACTAG TGTTGAACTG GGCCCAGAGC 1080
CAGCAGACTA GGGTGTGAAT GCACACAATA TACTGAGACA TCAACCAAGG CAGCTAAAGT 1140
GGTACCAGCA TTACCCCTCC TCTAACCCCA GGCTGCACAG CTCATAGTTC AAAATAATGA 1200
GACTCCTTCC TTCCACTTCA GGAGTGGAGA CAAAAGAGTA GGGAGGACTT TGTCTTGTAT 1260
CTTGGATACC AGCTCAACCA CAGAAGGATA GGGCACTGGT CAGTCATGAG GCCCCCTTTC 1320
CAGGCCCTAG CTCCCACTTG ACATTTCTAG GCACGCCCTG GGCCAGAAGG GAACCAGTTG 1380
CCTAGAAGGG AAGCACCCAG TTTTGGCAGG ATACATCACT GGCTAACTGA AGAGCCCTTG 1440
GGCCCTGAAT AACCAGCAAT GATATCCAGG TACTATGTCG ACGGCCTTGG GTGAGACTCT 1500
GAGACTTGCT GGCTTCACAT GAGACTCAGC ACATTCCTAA CTATGGTAGC TATGGGGTGA 1560
GACTTCTTCT GCTTGGGAAA AGTGGAGGGA AACGTAAAGG GGACTTTGTT TTGCACCTTA 1620
GGTACCAGCT TGGACACAAT GGGGTACAGA ACCAACTGGG CTCCTGGGGT CCCTGATTCT 1680
AGGACTTGGC TCTTGGATGG CATTTCTGAA CCTGCCCTGG GGAACAGTGG AGCCCACAGC 1740
CATGAAGGGT GAGTCCCAGG CCTAGAAGCA TTCACCACAA GCTGACTGAA GAGCCCTTGG 1800
GAACACTGGC AGTAGTGTGG CAGTACTCTC TGTGGGCCTG AAGTGGCGGT AGCCATCCGA 1860
TGAGGCTCTC CTGCCTTTGG AAAGCGGTAG AAAGAGTGGG AAAGTCTACA TCTTGTGATT 1920
TGAGTGCCAG CTCAGGTGCA GTACAATAAA GAACAGAACA CAGGGTAGAC TCCTGAGGTT 1980
TTTTACTCTA GTCTCTGACT CCTAGATAGC ACCTCTGGGG GCCTGGGGGA ACTTGTCACC 2040
CTGATAAGAA GACTCTAGTC TCTGACTCCC AGATAGCACC TCTGGGGGCC TGGGGGAACT 2100
TGTCACCCTG ATAAGAATGA CACAGGCCTG GCTGGCTTTG CTACCTGCTG ATTGTAGGGC 2160
CCCAGGGCCT TGAGCAAACA CAGGCAGTAG CTAGGCAATG GTTACAGAAG GCCTTGGGTG 2220
AGACCCAGTG CTGTGGTGGC TTCAGGTCTG ACCCAGCACA GTCCTTGGTG GCCACAGGGG 2280
TGCTTGTGTC ACTCCACCCT GAGCTCCAGG TGTCTCAAAA CAGAGAGATA GACTGTTTGG 2340
GAGAAAGTAA GGGAAGAAAA CAGGAATCTT TGCCTGGTAA TCCAGAGAAT TCTTCTGGAT 2400
CTTGTCCAAG ATTGTCAAGG TGGTACCTCT ACAAGTCTGC AAGAATCACA GTGTTACTGG 2460
GCTTGGGGTG CCCCCTAAAG CAGATTGAGC TTAGATCACA ACACTCAAGT CCTTTTGAAC 2520
ATCTGGAAAG CCTTCCTAAG AAGGACAGGT ACAAACAAGC CCAGACTGTG AAGATTACAA 2580
TACCTACCTC TTACAATTAA TAGCTAAATG CCTAGACACA GAGAAACATC TACAAGCATC 2640
|
| |
|
|
|
