Tag | Content |
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EnhancerAtlas ID | HS147-04204 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:201160040-201161550 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:201160636-201160647 | CTTCTGGGAAG | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 201160785 | 201161096 | chr1 | 201160901 | 201161255 | chr1 | 201160853 | 201161078 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I201191 | chr1 | 201160358 | 201162330 |
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Enhancer Sequence | TGGGTGCTCA CACCTGGCTG CCCACCCGGG CCAGGGTAGG GCCAGGATGG AGACACTAGC 60 CTGCTGTCCA GCTTTTCTAC GCAGGAAGGG GCAGGCAGTG GGCAGGATGT CTGCCTGGGG 120 AACATTCCCT GGCTGGCGGA TCACACGCTG GGGTGCACCT GTATCCCCTC TAGGTTACTC 180 CAGGATATCT GGAGGAGAGA ATTTCAGTGT GTCCTGTCTG GGCATTTCTG TCCTGGCTCT 240 AATTTTCTGG ACACGGCTTG ACTTTGGGTG TGATACGATG ACCAGATTAA AAATATCACT 300 AGCAGTCCAG AATAAGGACC TCGGGCTGGG ACTTGTTATA TTTTGGTTAG TATCATGGTC 360 AAAGCAGTTG AGAGAACTCC ATTTGGCTCT TCCTGCCTCA ATTTCTACCA GTTGAGAGGT 420 AGCAGGGACC AACTGGAGGT AGCAGGGACC TGGATGTGCA GGATGGATCC GGGGAGGGTA 480 GGGAAAAAGG ATGGGGAGCC ATAGGTCCTG GAGAGGGGGC AGGGAGGGAC TGTCCCAGGA 540 TCCAGTGCTG AGAGTGTTGT TGGGACAGCT GAAGTGAGGA CACAAACTGC TGTTTCCTTC 600 TGGGAAGAAC TGGAGTTCTT CTCAAATGTG GGAATGAATT ATGGAGGAGA GAATTCATTT 660 CCTTTCTCAT CCCTTCCAAC TGAGACTACA TCCCTCTAGT CTCCAATCCA ACAGATCTCT 720 TTCCCTGTGT CATTGACTTT GTACCAAATC TGGCTTATTC TAAAAGAGAG TGGAGCTCCA 780 GAAGTGGATG CTTAACGTCA CATCCCTAAG TTCCCCCAAG AGCTTTGCTT CTTTTGCCCT 840 CCTCTGCTGG GAGCTGTAGG CAGGAGGCTG GAGGGAGAAG AGTGGTATCA GCGTCATCCT 900 TCTTCATGTG TGACCAATAG CTGAGTAACA GGATGATAGC TGCTCGTGGT GATGATGTGG 960 GTGACGATGG GGATGATGAC TCAGATAGCT GTGTTGAACT CAAACTACTC CAGTGTGGGG 1020 GTCACCGACT GGCACCAGTG CACTTGCATC TACCAGGAGG CTGCACTGAG GGGTGGGTGG 1080 GATGGGGGCC CTTGCAGCCC TCCCCCTGGC CGTGTCCAGC TGGGTCCTCA TCCGTTGGTG 1140 GCTGCCTTCC CTCCCACCCT TCCTCGTGAC TCCCTTCGGC GTAGTGCCTG TGGCACCCGT 1200 GACCACTCCA GAACGCAGTT GGCGTACCAT GGCATTCCAG CACGCTAGGG TGCAGCGGCT 1260 GGGCTGGCGA GGGGCTGCCA GGGGTCAGAA GTGCCAGTGG GTGGCCGTTG CGAAATGGAA 1320 TGATCTCCAT GGGAGAGAGG AATTTGCTCT GTCATGTGTG ATTCTATATT AATGATAAGG 1380 CTCTTTGGGC AGAAAATGGA GTCCCCAAAA TGGAACCGCT TGGCCATGGG CCAATCGCAC 1440 AGAGGGTGGG ACTGCTGGAA GATTCTTTCA AGACATCCCC CCTCCCTGAT TTATGGCTCT 1500 CATCCCACCC 1510
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