| Tag | Content |
|---|
EnhancerAtlas ID | HS184-06678 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:118040900-118043490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:118042509-118042528 | GCGTGCCCTCTAGTGGTCA | - | 7.07 | | KLF5 | MA0599.1 | chr11:118041763-118041773 | GCCCCGCCCC | + | 6.02 | | Sox6 | MA0515.1 | chr11:118042617-118042627 | CCATTGTTTT | + | 6.02 | | TFAP2A | MA0003.3 | chr11:118041134-118041145 | TGCCTGAGGCA | - | 6.02 | | ZNF263 | MA0528.1 | chr11:118042374-118042395 | GGGGGAGGGCAGGGTAGAGAG | + | 6.01 |
|
| | 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 |
| GH11I118171 | chr11 | 118042057 | 118042766 |
|
Enhancer Sequence | AGAAGGATAG ACATCAACAA GGAAAAAAAT CATGGAGTTG TAGGTAGAGA CACTCGGCAA 60
GGTAGAGGGG CATTGTCTGA TGTCGGGTGG GCAGGGAAGA CTGCTCTGAG GGGGACACAC 120
AGGCAGCGCC CACCTGAAGT GAGAGAGTGA GCCCGTTGAA GTTTTGAGCG AGTCGAGTTC 180
CCAGGCAAGT GTACTCCCAG GGGCCAAGTC CCAGTGGCTG GAAGGAGTTT CGTGTGCCTG 240
AGGCAGAGGG AGCAGAATGA CCGAGGGGGT GCATGGTGAG ACCTGAGGTC CAAGAGTTAG 300
GCAGGGACCA GCTCACAAAG GCTTTGTGGG CTAGGATATG GAATTAGGAG TTTCCTCTTT 360
GGAGTGTGAT AGGAGGTCCC TGCAGGGTTG GGGAGTATGG GGGCTGCTGG GAGGCTGTCC 420
AGATGAGCCC GATAGAGGCT GATGTGGGAA TCGCATAGAC AAGGGGATGA GACTAGACTT 480
GGGTTCAATC CCAGCTCCAG CATCAGAAGC TGGAAGAGTG GGGGCTACTC CTTTGTAAAA 540
CGCAGTTGGT GACACCGATC TCCCAGGGTT GTTTCGATAA TGAAAAGAAG CAGTAAGTAT 600
TCAGCAAATG GTAGCTGCTA TTATCCTCAA TTCTCCCCAA GTTCTGCCTT GCAAACAGGA 660
AGGGCTTCTA GGGGAGCCTC TGGCCTGGCC TGAGGGCACC TTGGAGACTG CCCCACTCCA 720
ACCAGTCCGT AGGAATTGGC GAACAGCCCA GGCCTGCAGG GCTCCTATTT TTCAAACTTT 780
TTTTTTTTCT TCACAAAGCC GTAGAAGCAG CCGCCCTGCA GCCTGCAGGG AAATCAACAT 840
CTGCCTGGAG CACCCTTCTG CCAGCCCCGC CCCTGGCCCG AGTGACCAGG GCAAATGGCA 900
GGACTTAAGA ACCAGAGATT CTCTGAACTG GCAGCAGCCC TGGATGGAGG GGTAGGCATG 960
GGGACCTCAT CTGTTCTCCA AGCTGGGAGA CAGCTGTCAC CATCTGCGTT TTCTAGAGGA 1020
GGAGTCCAGG GCCGAGGATT CCAGGTGTGA GCTTAAGTGC TCATTAGGGG AATAAGGACT 1080
GGGGAGGCTG AGTGGGCCCC TGTCAGGAAG AACAAAGCCC AATTCCATCT CCTGTACTTT 1140
CATCGCCGTT CTGAAAGCAT CTGGCAGCGC ACCAGCCAAG GAGGAGGTGT GCAGAAAATG 1200
CCAACAGCAT CTTCATCTGC AGAGGCCCAG AGCTCTGAGG GAAGGCACTG ACAGTGCTTG 1260
TCCTGAGCTT ACCTCCCATC CCAGGAATGT CCTATCCCTC TAGCTCTTCC CTTGGAAGGT 1320
CGATCATCTT CCCAGGGGCT CCCCAGACCA AAAAGTCTGC GTTCTGCGAA GCCCGGCGGA 1380
CTCTGTGCGG GCCTCTGCCC CCCACCAAGC CCAAGGCAGT GCTCCAGATT AGAACTTGAA 1440
CCTCACCATC TCGAAGGAGC TAGCACCCTG CCGTGGGGGA GGGCAGGGTA GAGAGGAGTG 1500
CGGGGGCGCC TTTTCTGGCC GGCAGGACGG GGGCAGCCGG AGAGGTGCAA TGCGGGCTCC 1560
CCCTCCCCAC CCTGCAGCGG GGCCCTGCAG AAGGTACCGG GCGGAACACG CGTGCCCTCT 1620
AGTGGTCACA GAGTCAAACG TCAAGTTCCA TCCTGCGGAG CGAGCATGGG ATCCGGAGCC 1680
ACAGCTGGAG CTGAGATCAG AAACCGTAGA TCTAGCCCCA TTGTTTTACC GGTGAGGAAA 1740
GGCCATGAGA GCCACACACA GAGAATAGGG ACAAGCTGAG GCCAGAATCA TGGTTCCTAG 1800
CCCCTAATCC AATATCTCCA CGTAAGCCTG TGGCCTCACC AGAATCCCAG CAGCTCTAGG 1860
GTGCTGGCCT CAGACCTCCC GCCAGTCCGG GCCCTCATTA AAGACGAGGG GACCATGGCT 1920
CAACAAGGTC AGAGCTGTGA GCAAAACTCT GGTCTCTTGA TTAACTCTCC TGCTTCGGGA 1980
AAGCACCCGA ATGCATGGCC AAGGCCACAG AAAGGACTTC ATCACAGCCA CAAACCCTTA 2040
CAAAATGCTT ACAACGAGCC AGGCACTGTC TACATACTCT ACATACATCA CCTCATTTAA 2100
TACTAACAAA ACCTGTTATC GCTCCCACAT TCCGGATGAG GAAGATGGAG CACAAAGAAG 2160
TTAAGAGACG AGCCCAAGTT CACGGCTAGT AAGAGGCGAA GCTAGAATCT GAAGCCAGCC 2220
TGCCTGGCTC CAGACTGGGT TGAGGCATTG AAGCTGAGTG GTGAAGTGAG CCCCATTCCA 2280
AGGCATCCGA TCTCTTGCCG ACTATATGGC AGGTCCAACT CCAGGCAGGC CCGCCAGCAG 2340
GGAATTGTAC CATTTAAAGG AACCTCCATA CAAGGGGGGC CCACAATCTT CCTGGTTGTC 2400
CCATTTGAGA CCAGGTCTGG GGCCTGTGTC TCCTGATTTT CAACTCACAG AAGGGAAAAG 2460
ATCATCAACG GGATGAGGCT TCTGATCTTA GATCCAAAAC CTCAGCAGTG GCGGGCCACC 2520
CGCTGTCTCC AAGGCACATC TGGGCCCTCA GGCCTCGTGT CATCCACTGT TCTAACTAGC 2580
CCATCTTGCA 2590
|
