| Tag | Content |
|---|
EnhancerAtlas ID | HS091-32135 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr21:38226450-38227650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr21:38226901-38226914 | CAGAGGTCACAGG | + | 6.19 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAACGTCAAT ATTTGTCATA TGTTAAAAAT CACATCCTAC AATTAAGCTT TTGATGAGAA 60
CTGTTAGATG TCAGCTTAAA CACGTGTAAG GGGATTTACA GATTTTCAAA ATTATTTTAG 120
GGGTACACAA CTAAGAACAC TGAACAATCA CTGCTATAAT GGCACCCTAT TACTCTACCA 180
CAGGAACAAA AGCTCCCGGG GTTCCCACCA GAGACAGGCA CATCTGGGGC ACGGGGAAGG 240
ACGCTTAGAG TGATGCTCAT TTAAAAAGCT CATTTTAACA GGGAACAGTA AGACAAGCAT 300
CAAAAGGAAG TGCAGACTGT ACAGATCCTT GGAGCTCTGC AGGGGGAGTG ACTTCTTAGG 360
CGCTGGTTTT CCTCCTGTTT ATGAGAGTAG GACTAATAAT TTGAGCAGTT CAAGGTGGGG 420
AAAAGCTTAA GTACTGAGTG CACTGAGGAA GCAGAGGTCA CAGGAAGGAC CCCATAGCGA 480
GGTCCTCTGT GGGTGCAGGA CTGCCCCCTA GGGGACATTT CAGAACTCTA TTTTTCTGGT 540
TGTCATAATG ACCAGAACGT ACTGCTCAGA GGGGCCAAGG ATTCACGATG TCTTGCAACA 600
CACAAGGTCA GCCCTGGACA ACAAGATTCT CCCACTATTA AAACAAATTT TTAATATTCC 660
ACTGGACACA CATTTAGATG AAATACTTGT TCACAATGAT CTGACTTGAG AATCTGATTC 720
TATTTTTGCG GGTACACAGC AAGTACTTTC TGTACAGCGG TATTAAACTC TAAATATTCC 780
AAAGATAGGA CCACCATGTA AATCAAGGGG GAGTTGGGTA AAGTCCATAC AAGCACAATC 840
TGTTTCGCAC TCTGAGACCA GATCATCTCA GGCTACACTA TTCATAGTGT CCAGGCTGCC 900
CAAGACCTTG CAGCCATCAT ATTCATGTTT TTTTTTTGTA TAGGTGCATG TGTCTATTTC 960
ATCACATCTT CTTAACAGTC AGATATGAGC ACATATTCCG ATGCATATTA TTTTCTTTAA 1020
CTTTTTATTT CTATATTGGT TTTTAGAATT ATCTGTATAG ATCGTTTATA TAATGTATAA 1080
ATCCAACTTC AAGAAGTTGG CCACGCATGG TGGCTCACGC CTGTAATCCC AGCACTTTGG 1140
GAGGCCAAAG CGGGTGGATT GCCTGAGGTC AGGAGTTCGA GACCAGTCTT GTCAACATGG 1200
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