| Tag | Content |
|---|
EnhancerAtlas ID | HS129-37667 | Organism | Homo sapiens | Tissue/cell | MCF10A | Coordinate | chr9:111548600-111550890 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HLF | MA0043.2 | chr9:111548778-111548790 | GATTACGTAATG | - | 6.37 |
| | | 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 |
| GH09I108786 | chr9 | 111548725 | 111550850 |
| Enhancer Sequence | GAATAGTTCC ATCTCAGGGA TCCCCAGTGC TACCACCCTT TTATAGAACC ATTAAACAAA 60
GAGTGGTACA TCTAAACATG GAATACTACT CAGCAATAAA AGGGAATCAA CTATTAATAC 120
ATGCAACAAC TCCAACGGAT CTCAAGGACG TTATGTTGAG TGAAAGCCAA TCTCAAAGGA 180
TTACGTAATG TATCATTCCA TTTATATGCC ATTCTTGAAA TGACAAAATT ATAGTTACAA 240
AACAGATGAG TAGTTACCAG AGCTTAGGGA AGGGAGAAGG GAGGGAAGTA GCTATGGCAG 300
ATGAGGGACA TGAATAACAC AAACCAGAGA ATCCAGCTTA TTCCAAGTGC AACGCTGCTT 360
TCCCAAAACT TCAATCCTCA CCCTTCAACC TTACTACCCT ACCGCATCCC ACTGCCACCC 420
CTAGCAGCTG CCTCTTGCTG CTTTAATATC TAGTAAATTA GCAATGGCTT GGGCCTTAAT 480
GAAAGGACCC TATTGATAAT GGACCCTCCC TACTGGCATC CCAATAGGGT GTCATCTGTC 540
CAGTGGAAAA GGGAGCTTGC CCCTGCATTC TGTGACTCCT TTTCATTCTC TTGAAGACCT 600
CCTGGAAGAG CTGAGAGCCC TTTGACATAC TTAATGCATG AGCTGTCTTG TGAGCTTGGG 660
AGGATTACTT GGCTTTTTTT TTTTTTTTCT CTTGCTTCTG TTTCTTCCCT AGATGTAATT 720
CTATTAAACA GCTTTAAAAA TAAATATGTT GCTGTGGGAG GTTGAGTGAG GGGGTAGTTA 780
GTATGACATT TCTGTTATTT TGAAATTAGA CCCATGGGAA GCCTCCAGGC ACACAGTAAA 840
GTCTGACATA ATCCACTTAC AAAGGAGATT AAGGATGCTG ATGAGCTCAC ACAGGCAACT 900
CCCTGATGTA CTCACGGATG GTACAACTGA GCCCCAGGAG CCAAATAAGA AGAGAAGGTG 960
CATTTCACAA ATGCACACCA GGGAGATAAA TCCATGCCCT GTAGAGAGGT GCACCATGCC 1020
TCAGCAACAA CCAGTCCCTG AATAAAACTT CAAATGGACT GAGAGGCTGT GAGCCAGACC 1080
CTGCAGTTCT GGCTGCACAT ACATCTCTGT AGAATGGAGA CTACCTTTGA GATGGGGGGA 1140
AGGGCTTCTC AGATGAGGGA CATTTGAGCT GAGCCGAAAG AATGAGTCAC TTGCCAGGCA 1200
GTAGTTCGGA GTGGGGCGTG GTATTCCACA CAAGGGGAAC AGCATGAGAA AAGGGGCTGG 1260
CTGGCATGGG GCAGGGAGAC TTGGAGCAGT CTGGTGTGAC TGGGAAGTAC GACATGCTGG 1320
GGGAAGTAGG GGAAATTGAA ATCAGTGGAG GGCTTGCCTG TTATGAAGAA TTCGGCCTTT 1380
AAGCATGAGC AGTTTTGAAA GCACCGGTGT GACATGGGAT TTTAGAAAGA TGACTCAAGT 1440
GGCCCTGTGC GAGCAGATAC ATTGCAGAGG CGAGCCTCTG GTCTGAGAGA GGTGAGGAGC 1500
CCCCTGCCTC CTCTCATCCT CCTCATTAAT GAGAATGAGA CAAAGCTCCA GCTTCCTGGG 1560
AGATTTACAT GTTAAGGTGG TTTGGCGGGA AGTGCTGCCT TCTCGTGTTA AGACGGGACT 1620
TGTCAGAACA AGCACCTGGC TTTGGCTGAT GAAAAAAATA AGCAAGCACA GTTTTAATTG 1680
CACACAGTTT TAAGAGGGGT GGGGGCTCCC AGCTTGAGGC TGCAAGATGC AGGCCTTCCT 1740
GAGTCTATAC AGTGAACCAT CAGTGGGCCA CAAGGGTGCC TTGAGAAAGA GCCAGTGCTG 1800
AGCCCAGTGC TGGGTAGTCG GGATGTCTGG CTTATCCAAC AGAGGGGAAG CAGCCTGATG 1860
GTGTCTATAT GGAGGACTGT CTAAGGAGCC TCCTGGAAAG GGATATATCC TAAGGGAAGG 1920
AAGAGCCTAT TAGGCTCTAA GGGTGGGATA CAATCTCTTA ATTCTGAGTT CAGGGAGGTA 1980
TCTGCCTATC CAATTTGTCT CTTGACTCAG CTTCCATTGG GTTCATGTCA GAGTGCCCAG 2040
TGGAGCAAGA GGCTATAAGT AAAAACAGAA ACACCTTGGG ACTGGGGCAG CCCTCCTTTG 2100
GGGACCCTCT AACAGAATGT GGCAAAGATG AAGGAAACAG TCTTCCTCCA CACACCTGAC 2160
ACCTGAGGGC TTGGGATGGC AACGGTAAGG AACTTCAGGA GAATTACAGC CATTTACAGA 2220
CCAGCACAGA GCAGAACAGC ATTTCAGCCA TACCTACTGT CGTAGTCTGT TCAGGCTACT 2280
ATAACAAAAA 2290
|
| |
|
|
|
