Tag | Content |
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EnhancerAtlas ID | HS184-00749 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:47943130-47944640 |
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 | CCTTCATTTA ATCACATCTG CAAAGTCCCT TTCACCATGT AAGGTAACAT ATTCACAGAC 60 TCTGAGGATG AGGATGTGGA CATCTTGAGG GTGGGGAGCA TTATTCGGCC TCCCACACCA 120 TCTTGCAGAT GAGAAAACTA AGACTTACAA AGGTCAAGGA ACTTGCCTAA AGTTCTACAG 180 CCAGTAACTG GCAAGTCCCG CCCTCTTTGG ATTTGAGCCT CCAGCTCTTA ACCTCAAACA 240 AGAAGACTGC TGGTGCAGGT GAACCTTGAA CTAGGTTTTG AAGAATGAAT CAGAGTTAAA 300 AAAAGGTGTG TCCAGTGGAG GAATGGTGTA TGCAAAAGCA AGCTGAGCAC TGGGTGTGCT 360 TTGGTACCAT AAAATGCTCA GATTCGCTGG GGGTGCAGGG AGGTGAGACA AGACAGGTAG 420 GCAGGGTCTG GATGGTGGAA AGCCGCCTAG AGCAGGCTAC AATGTTTGCA GTTGAATTGA 480 AAGATGTGAA AAACCATTGG AGGATTTCAC CTGTATGTCC TGGGTAATCC CTTCCCCTTT 540 CTGACCCTCA GTTTCCAGCT CCTCTGCCCT GATCTGCTTT TTCCCTCCCC ACTGTCCCTT 600 TGTCCCCTCC CTTCTCACCC CCTTGCTGCC AGGCCTGGTC CCATCCATCC CTGGGCAGGA 660 ATGAGGGCTG GGTGAACTGC CCCCTTCCCC CATCCCCAGG ACAGCGACGG TTTCCAAATA 720 TCTGTCTGTT GAAATAATGT TCTCTGGGCA CTGGGCCTCC CTCCCTCCCT CACATTCCTG 780 GGCGAGCCGG CCTGTTTGGC TTGCTCGGAC AAATATTGAC TTTCTCTGTC CTTCTCACTC 840 TGGGTCTGTT TAAAAGGCAT CAATCTTTGC CGGGGTGTGA GCTCCCTCTC CGTAACCTGT 900 GGCCTCTGCG GTCCTATTCG GGCAGGGAGT GGTAGGGGAG GGGCTCACAG GCTCTGGGGA 960 TACCCCTTTC TTGCTTGGCT GCACTATAGA GGCTTTTGGT GCAATGCTGT TCCTTGTCAG 1020 CTGCTTTCCA CGCGGTCCTG CGTGGGGCCT AACAGCCCAC TTATGGAGCC TCTACTTGAG 1080 GGTCAGGTCT ATGCCCGTGG CATGTGCACT GAGACCTTCA TACACATTTC TCTAGACTCC 1140 TCAATAACCA GGCAGGAAAC CCTGCTGATT CTACCCTCAA ACAATTATTC ATCATCCAAC 1200 CACTTCTCAG CCTCCACCGC TACCCTCCAG GTCCCAGACA CCATCATCTC CTGGATCTGA 1260 CTCCTGGATT ATTAAGTTAA CTTCCTAAAT TCTGCCCCAC TTCCCTTCAG TCTGTTGTCA 1320 ATTTTGGAGC CAGAGGGATG GGTGAACATG TTGGTTAGCC TGGCTTAGAC CCCCCAGCTC 1380 CCCTCCCCTC CTCTTGCTCC TCCTCTCTCC CTTTGGGCCT CAGGGTTTTT CCTCCCACCT 1440 GAAAAACTTT GCACGAAACT GTTCTCTCTG CCTGGAACGG TCTTCCCAGA TCTGGTAGAT 1500 TCCCTCCCTT 1510
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