| Tag | Content |
|---|
EnhancerAtlas ID | HS129-10640 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr13:77510530-77512370 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr13:77511659-77511670 | ATGTTTACATA | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 77510530 | 77510626 | | chr13 | 77512091 | 77512174 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I076936 | chr13 | 77511001 | 77512428 |
|
Enhancer Sequence | AACGGTCTGA GATGTTGCCC TACGTGCAAG CTAACGGGTA AGCCTATCGC AGTTTCATGG 60
ATGGTGGCAG AAGACTTGAG ACTTCTTGCT TTTGGACTTG TTTTATTTTT TTAATCATCT 120
CATTCCTCAG ATGATTTCCT ATTCATACTT CAACTTTTTA CTAATTATTT ACCCGAAGAT 180
TTTGATACTT TAAGACATGA TCAACTCCAT ATACTACTGG GCCTAATCCT CGTTATTGGC 240
ACATTGAAGC AACATAAGCC ACCTCAGAAC TGAGAAATAC AGATTAAACT AGCCAAATCC 300
ATGACAATGA CTGAGTTGTG TACAAATGAC CCATACCAAG TATTAGATGA AACAAGAGAC 360
TTCCAAGAAT TGGCATGGCC TCAGGGAGAC ACAATGTGCC ACTATGTCTG AAGATGTGCC 420
ATAACTGTTA AGCTGCCATC TTACCAGTTA CAAGAACTCA AGTTTAATCT CTTGCAAGAA 480
CTATACTGAA AAGATGGCCT AACAACTATG TGCTGTCACG TGTCTGAGTG TTGCAACAAC 540
AGGTGAATGA TTAGTATGGA ATTTTAAAAG GGGAACAAAG ACAAAGAAGG AACAGAAGCT 600
AACTAGCATA AACTGGGGAG AATTTGTATC TGGCAAATAC CAACAGAGAA GTATCTGCTA 660
TGTTGGGGCA GGGACTTCCA ACTGGCTTTC CCAAGGCCTT GGTAAATGTC CCTCCAATCC 720
TGTGACGGTT AATTTTATGT ATCAACTTGA CTGAGCTAAG GGATGCCCAG ATAGCTGGTA 780
AAACATTATT TCTGAGTGTG TTTGTGGGGG TGTTTCTAGA AGAGATGAGC ATTTGAATCA 840
GTAGACTGAG CAAAGAAGAT CCGCCCTCAC CAATGTGGGA GGGCATCATC CAAGCCATTG 900
AGGGCCTAAA TAGAACAAAA TGTCAAAGGA AGAGCAAATT TGCTCTCTTC CTTCTTGAGC 960
TGGCACTTGC ATCTTCTCCT GCCCTAGGAT GTTGGAGCTT CTGCTTTTCA GGCCTTCAGA 1020
CTTGGACTGA ATTACACCAT CTTTTAGTTC TCCAACTTAC ATATGGCAGA TTGTGGGACT 1080
TCTTGGCCTC CATAATCATG TGAGCCAATC CCCATAATAA ATCTCTTATA TGTTTACATA 1140
TATCCTATTA GTTCTATTTC TCTGGAGAAC CATGACTAAT ACACCCTCCC ACTGCTTCAT 1200
TCCAGTTCCA CATTTGGCAA GCAACATTCC ATGACTCATC TGGCTTCCCA GCCATGTTGC 1260
TATAGGGAAG GACCCCAGAT AATGAAAGAA ACTAGCCTTG CAATATAAAG GAACTAAAAT 1320
GATACGTTGG CATTCTGATC TATGCATCAG ACTCTCACCA GTTTGTTAGT GAGACTGTCA 1380
TTTCCCCGGT GGCAGATTGC CTGTAAATCC TCAGTACTAA AGCTGGATCC AGCCATGGAC 1440
ATGCAGCTGA CGACATGAAG GCATTTTCCC AAGAAGGCCA CCTGGCCTCT CTAAACTCCC 1500
CCTCATTACT CCCTGATAGC AACTGGTCCC ACCCCAGGTT TCATCCTATC CTAAGGTGAG 1560
TGCCTGAGCT GAAACTGGTC CCTAAAATTC CAGAAGTCTT TGGAGACAGG GCAATTCTAA 1620
ACCCTTCAGG GAAGTCCCTG TTGTCCAATT TAGGACATGC AAGCAGAATG TCACTCTCAA 1680
GACTGAAATA TTACTTCTCA ACTGTTTAAA GACCAGAATG GGATGAGGAC TTGGAACTGC 1740
CATATGCACC CAGGATCCAT ATTTATTCAT TCAGCACCCA GAATGTGGTA GATAATAGAT 1800
ACTATAGATA CAGAGGAAAA TGAGATGGAA CATTAACCAT 1840
|
