| Tag | Content |
|---|
EnhancerAtlas ID | HS091-30486 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr20:30848020-30849220 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr20:30848159-30848174 | CGAACTCTTGACCTC | - | 6.24 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTTGGCCAGG CTGATCTTGA ACTCCTGACT TCGTGATTCA CCCGCCTGGG CCTCCCAAAG 60
TGCTGGGATT ACAGGCGTGA GCCACCACAC CCGGCCATTT TTGTATTTTT AGCAGAGATG 120
GGGTTGGCCA GGCTGGTCTC GAACTCTTGA CCTCAGGTGA TCCACCCGCC TCCGCTCCCA 180
AAGTGCTGGG ATTACAGGCA TGAGCCACCA CGCCGGGCCA GGACTTTGTT TTTAATTATT 240
AGAAGTACAG CTCACATTTT CCCTTTAAGT GCCAGAAATA CGACATTTTC CTTTGTCCAC 300
AATGCAGATA AAACTCAGCT GAGTGAGGAT GTCTGCAGGA TCCTGCTTCT TTGGGATGGT 360
GGGCAATGAA CAACTATGGA CATAGGTGTG TTGTTTGTAG GTGAAGAGAG GGGTTTAGTG 420
GAGAGGGCAT TCTAGGTGAG GAGAACCGGT GGAACAAAGT ATTTAGAGGC GGGTGAGCTC 480
CTGGAGCCTG ATCAGAGAAA AAAGGGAAAT ATCGCCAATA CTTAAGTTGG GCCTGGTGTT 540
GACAGGAAGA CAACCTGGCC TAACCTCTGG AAAATGGGGA GCCATTAGAG AGATGTAAGC 600
AGGGCAGTTC TGCAGAAACA CACAAAGAGG GCTAACCAAG AATGATCACG GTTTGCAAGT 660
CACTCACTGA ATGTGCTTCT GAAAGGACTC GTCTCAAATC AGTTATATAT TGTGTCTCTT 720
CTCCAGAGTC TGGGAGCCTC CAGGGACGAG GGGAATAGGA TATTTTTCAT CTCTCTGTCC 780
TAGAAACACA CCCAATATTT GCAGAGGACT TGAGAGAAGG GGAGGGACTG AGCTGGGGTC 840
ACCTGATTGT AGGCAGAGGA GAGAGTGTGA GCTCTGGGTT ACAACCTGAC TCTGCCACGA 900
GGTAGCTACA CAACCTTGGC TAGTTAATGA ACTGAGCCTC AGTCTTCCCA TCTGTAAGGT 960
GGGGATAATA ATAGTACCTT TGGGCCGGGT GCGGTGGCTC ACGCCTATAA TTCCAGCACT 1020
TTGGGAGGCC GAGGTGGGCA GATTACCTGA GGTCAGGAGT TCGAGACCAG CCTGGCTAAC 1080
ATGGTGGAAC CCCGTCTCTA CCAAAAATAC AAAAATTAGC TGGGCATGGC GGCGGGCGCC 1140
TGTAATCCCA GCTACTCTGG AGGCTGAGGC AGGAGAATCG CTTGAGGTGG GAGGCGGAGG 1200
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