Tag | Content |
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EnhancerAtlas ID | HS146-14244 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr8:50728990-50730140 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat4 | MA0518.1 | chr8:50729737-50729751 | CAGTTTCCTGGAAG | - | 6.35 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 50729183 | 50729890 | chr8 | 50729196 | 50729781 |
| | Number: 1 | ID | Chromosome | Start | End |
GH08I049816 | chr8 | 50728881 | 50731516 |
| Enhancer Sequence | AACAACAATG CCTTAATATT TCTTATTTCC TAATTTACAC ATGGTCACCG CTCTGTCAGC 60 ATTTCTACCC TTAACATCAA TACTAATTCT ATATGTGTGT ATAAGTTAAA TGTAGTTGCA 120 TAGACCCATA AATGGCCAGT TTCTCTTGGC TTCACCTATT TGTGGGTAGA ATTGTATTTG 180 TGTTTGAAAT AATCACTCAA ATTCTACTGA GTTTTGCCCC AACATGCACT CACGACTCCA 240 GAAAAGTTCC TCTAACTTTT CAGCAACACC CGCATGTAGA GGCCAGACCT CTGCAAAAGG 300 CCCAAAACCC TGCTAGACTC AGGCTCCAAC TTGCCCACTT CTCGGGGCAG AGCTGCCACT 360 TCCACGAGGT GCTCCTGCTC CCAAGGGGCA GTGACTATGT TCCTGGGCAT CCCATCCTCT 420 CTCATCATTT TTCTGTTTCT GAGCTTTACG ACATCTGGCA GACTCCCCTG CCAAGCCCTG 480 CTGAGTGAGG CTGCTTAGTC ATGCACAAGG AGTGATCAGT GCAGTGGTTC CTGAGAAGGA 540 GGGTGCTGTG CTGTTTCCAT TGCTTTAGTA CCTGCATGTA GATGGTGTTG TGTGCCTTCA 600 TGAAACAGCA TTTGCATCAT GTTCCATAGT GTCTTTCTTT GGCAGCACCC AGTGTTATAG 660 CATGGCTCTG ATACCAGCTG TGCTGAGCCC CTCTCTCTCT GGCCTCAGTC CCTTACAGGA 720 TATAAATTTC TTGTGTGTCT TCCCAGCCAG TTTCCTGGAA GGCCCATGCA TACTGAAACC 780 TAAGTTTAAG CATGCTAGGG CCTACCAAAC ACCTATCTGT ATACATTTAA AGACGGCCCA 840 AGTGAGTTTT GTTTTTTCTC TTTTAACCAT GATTCTCAAT CTCTTCTGTC CTCGTCTTGA 900 AAAAAAAGAA AGAAAATAAA GACAAGCATT TGTTGTAGTG AAATACAAAA CTCAGAATAC 960 TATAACTTAC CCTGAGCATC TTCAAACACA GCAAAATGTT CTGAGGACTC TACTCTAAAT 1020 ATCTTACATT GTTGCTTGGC CACCAGGTGA ATCCATATCG TTGTTATTTG ATTGGAAATC 1080 TTGAGTTGAG CTCATAGACA CCAGTAAGAC AAGTAGAGGT AAATCAGTAT GAAAAATATT 1140 CTGAGAATAT 1150
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