Tag | Content |
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EnhancerAtlas ID | HS147-35734 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr6:36923530-36924910 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr6:36924085-36924096 | TGTGACTCATT | + | 6.62 |
| | 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 |
GH06I036956 | chr6 | 36923777 | 36923977 |
| Enhancer Sequence | GCACACAGGA GACAGAAGCC AGATTTAGGG TTGGTTACTT CTGTCAGGAA GAGCTATTTA 60 TGGTAGGGTG AGAGGCGGGC TGTCTATATG CAGAATTAAA GGAGATAAAG TGAGAAATTC 120 ACCCACTTCC TGCCCTCCCT GAGGGCTGAA CTAGCTTGTC CCCTCCAGCC ACCCTCAGGT 180 GACTGGGGAG GTTGCTGGGC AGTGTTCAGG GACCCCTGGA GCTGGTGCCT GAGAGAACAG 240 ATGCACCTTG GGGAACATAA CAGTGAGCCT GGGGCCCCAA ACCTAAGTTC TAACCTCAGC 300 CTAATGTGAT CTGGCTGAAG TAACTCTGGG TGGACCCCTT TCCCTTCAAA GGCCTCTGTT 360 TCCAGATGGA AACATGGGGC TGGCGATCCC TGCCCTGGGC GTCAGACAGG ATGACACGTA 420 AGAAAGATCT AGGAAGAGCT CTGCACACAC CCAGCACTGC CGTTCACAGC TGTGCCAGCC 480 TGCACATCGA GGAAAGGTGG ACAACAAACC AGGCGTCACA GATGCAGCTC TGCCAACAGC 540 TCCCTGATTG AGGCCTGTGA CTCATTGTTG GACTTCAGTT TCCCCACCTG TAGATCCCTG 600 ATGCCCTACA GTCTTGCTGG CTGAGACTGG GGGCCACACA GGCTGGGAGC TGCTTCTCAG 660 ACAGAGGTGC GCCTTGGAGT GGGGCAACAT TCTGGGAGGC AGTTGGGATA CTGAGGGGAT 720 ATGCTGCTGC CTAATGGGGA GTGACATGAG GAGGAGGAGA TGAGGCTGGG GCTGGGATGC 780 CAGGAAACAT TCAGGACAAG ACTCAGGTTC AACCTCAGCA GTGGTGAGGG CAGGGACTCT 840 GCAGCCAAAT GGCCTGGGTT CAAATCTTAG CTTTGTTACT TATTAGCTTT GTGACCTTGG 900 CCAAATTAAA CTCTCTGTGC CTCAGTCTCC TCATCTGTAA AATGGGGATG ATAACAGTGG 960 GATAATTCCC TTGTAGCTAC AGTGGTTGTA GGGTTAAGTG AGTGAATATG TGTAAAGCAC 1020 TCAGAAGAAT GCCTGGCACA CAGTAAGTGC TCAGTAAGTG TCTGATTAAC ACAAAAGAGG 1080 GAATGGATCC AGGGTGAGGC AGGTGGGGGT TATCATGAAC TCTTCCTTCT CTCTCAGCCT 1140 CCAGAGCTAA TCAGCACCAG TTTTGCCACC CCGAAGGTTC AATTGTCCTT GAAATCTAAC 1200 CCTTACCCCT ACCCCCTTCT CTTTTCAGCA CAATCCTGGT TCAGGTTTCT TTCATTCTTC 1260 CACACAAGGA CTCCTAGGAT AGCCTCTACC TGTTCCCCAG CTTCTGGCCT CTGCTGTCAG 1320 AATGAATAAT CCAACACATG GGCCTGACCC TGCTCAAAAT CCTTCAGTGG CTCCCATGGC 1380
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