Tag | Content |
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EnhancerAtlas ID | HS129-01107 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:47943160-47944580 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP2 | MA0516.2 | chr1:47943320-47943337 | GCAAGTCCCGCCCTCTT | + | 6.38 | ZNF263 | MA0528.1 | chr1:47944509-47944530 | CCCCTCCCCTCCTCTTGCTCC | - | 6.88 | ZNF263 | MA0528.1 | chr1:47944515-47944536 | CCCTCCTCTTGCTCCTCCTCT | - | 7.82 | ZNF263 | MA0528.1 | chr1:47944512-47944533 | CTCCCCTCCTCTTGCTCCTCC | - | 8.37 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I047477 | chr1 | 47942901 | 47944366 |
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Enhancer Sequence | TTCACCATGT AAGGTAACAT ATTCACAGAC TCTGAGGATG AGGATGTGGA CATCTTGAGG 60 GTGGGGAGCA TTATTCGGCC TCCCACACCA TCTTGCAGAT GAGAAAACTA AGACTTACAA 120 AGGTCAAGGA ACTTGCCTAA AGTTCTACAG CCAGTAACTG GCAAGTCCCG CCCTCTTTGG 180 ATTTGAGCCT CCAGCTCTTA ACCTCAAACA AGAAGACTGC TGGTGCAGGT GAACCTTGAA 240 CTAGGTTTTG AAGAATGAAT CAGAGTTAAA AAAAGGTGTG TCCAGTGGAG GAATGGTGTA 300 TGCAAAAGCA AGCTGAGCAC TGGGTGTGCT TTGGTACCAT AAAATGCTCA GATTCGCTGG 360 GGGTGCAGGG AGGTGAGACA AGACAGGTAG GCAGGGTCTG GATGGTGGAA AGCCGCCTAG 420 AGCAGGCTAC AATGTTTGCA GTTGAATTGA AAGATGTGAA AAACCATTGG AGGATTTCAC 480 CTGTATGTCC TGGGTAATCC CTTCCCCTTT CTGACCCTCA GTTTCCAGCT CCTCTGCCCT 540 GATCTGCTTT TTCCCTCCCC ACTGTCCCTT TGTCCCCTCC CTTCTCACCC CCTTGCTGCC 600 AGGCCTGGTC CCATCCATCC CTGGGCAGGA ATGAGGGCTG GGTGAACTGC CCCCTTCCCC 660 CATCCCCAGG ACAGCGACGG TTTCCAAATA TCTGTCTGTT GAAATAATGT TCTCTGGGCA 720 CTGGGCCTCC CTCCCTCCCT CACATTCCTG GGCGAGCCGG CCTGTTTGGC TTGCTCGGAC 780 AAATATTGAC TTTCTCTGTC CTTCTCACTC TGGGTCTGTT TAAAAGGCAT CAATCTTTGC 840 CGGGGTGTGA GCTCCCTCTC CGTAACCTGT GGCCTCTGCG GTCCTATTCG GGCAGGGAGT 900 GGTAGGGGAG GGGCTCACAG GCTCTGGGGA TACCCCTTTC TTGCTTGGCT GCACTATAGA 960 GGCTTTTGGT GCAATGCTGT TCCTTGTCAG CTGCTTTCCA CGCGGTCCTG CGTGGGGCCT 1020 AACAGCCCAC TTATGGAGCC TCTACTTGAG GGTCAGGTCT ATGCCCGTGG CATGTGCACT 1080 GAGACCTTCA TACACATTTC TCTAGACTCC TCAATAACCA GGCAGGAAAC CCTGCTGATT 1140 CTACCCTCAA ACAATTATTC ATCATCCAAC CACTTCTCAG CCTCCACCGC TACCCTCCAG 1200 GTCCCAGACA CCATCATCTC CTGGATCTGA CTCCTGGATT ATTAAGTTAA CTTCCTAAAT 1260 TCTGCCCCAC TTCCCTTCAG TCTGTTGTCA ATTTTGGAGC CAGAGGGATG GGTGAACATG 1320 TTGGTTAGCC TGGCTTAGAC CCCCCAGCTC CCCTCCCCTC CTCTTGCTCC TCCTCTCTCC 1380 CTTTGGGCCT CAGGGTTTTT CCTCCCACCT GAAAAACTTT 1420
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