| Tag | Content |
|---|
EnhancerAtlas ID | HS091-11845 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr13:50180750-50182150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr13:50181198-50181219 | CCTTCTTGTTCTTTCTCCTTC | - | 6.35 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 50181000 | 50181347 | | chr13 | 50181023 | 50181976 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH13I049606 | chr13 | 50180937 | 50181950 |
| Enhancer Sequence | ATTCTTTCTA AAAATTAATT TCCTAAACCA TGTAGTTTAA TGTGATTTAA TGTAGTTAAA 60
TACTAGCATT AAAACTTGTT TCTTGAAGGG CGCAGTGGCT CACACCTGTA ATCCCAGCAT 120
TTTGGGAGGC TGAGGAGGGC AGATCGCCTG AAGTCAGGAG TTCGAGACCA GCCTGGCTAA 180
CATGGCGAAA ACCCATCTTT AGTTAAAATA CAAAAATTAG CTGGGTTTGG TGGTGCATGC 240
CTGTAATCCC AGCTGCTCGG GAGGCTGAGG CACAAGAATT GCTTGAGCCC GGGAGATGGA 300
GGTTGTAGTG AGCCGATATC GCACCACTGC ACTCCAGCCT GGGCTACAGA GACTCTGTCA 360
AAAAAAAAAG AAAAGAAAAG AAAAGCAGAA ACTTGTTTCT TGATGAAGTT TGTTTTCCTG 420
GGATCACACA CAGATCTCCC ACGGTGGTCC TTCTTGTTCT TTCTCCTTCT GCAAAGACCC 480
TGGAAACCGC TTGTTGAAGA TGGCGGGGCC ACAGAATGAA AGGAGCCTTG GTCCCTGAGT 540
CACGGCTTGG AGGAAAGCTT TATGGCGTTT AGGAACACTA TTGTTTGTTG GTCCTGAAGA 600
GGAAGTACTT CACAGAGCAA GCCTGCCACC ATGTGGCGCG GGCCCAAACC TAGCATCAGT 660
TAAAGGTTCA TTCTCATTTA CTTGGTTGCC TCTGGTTCAC TTACTAACCA ATCTAGATTT 720
AATGCTGTCT AATAAGAAAT TAATACCCAG GTGTATTCTA TAGGTTTAAG TAGTTTTTAA 780
TTTCAAGATA CATTTCTTCA ATTCTGAAAT TATTGCAATA TTTCCAAACT GGCTACAGGA 840
GTGACCACAA CATTTATAAT ATGATCCAGG CACATTCACA AGAGGACTAC TTCAGTGCAT 900
CACAAACATG GAAACAAACT CAGCAATTTG TAGGATTTAT CTCAGTTCAC TCAAAAGTTG 960
GTCAATGAGC CAGATTAGAA GGCAGAATTC CGGCCAGGTG TGGTGGGTCA TGCCTGTAAT 1020
CACAGTGCTT TGGGAAGCTG AGGTGGGAGG ATTGCTTGAG CCCAGGAATT TGAGACCAGC 1080
CTGGGCAACA GGGTGAGACC TTGTCGCTAT AAAAAATAAA AAAATAAGAG GCAGAATTCC 1140
TTGGAATGGA AACAGGTAGT GTGAAGGACT GCCAAAAATG GATGAAAAAC CCTCATGGAA 1200
GGAGAGTCAG AACTTAACAG TTTCCTAGAG TTTTAACACC GTATAAGCTC ACTATGTTCT 1260
AGCATGCCAG GCTGACGTTT CCCAGAACTC TCTCTACATT TATCAAGACA GGAATGACAT 1320
CGGAAGTTGT TTGCAAGACT ATAGGTCTAG CAGGTGGCTA AGAGGAAGTC TGGTATTGCT 1380
GCTGCGTCTA TTTTTATGTA 1400
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