| Tag | Content |
|---|
EnhancerAtlas ID | HS091-21688 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:80732000-80733650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:80733021-80733040 | CAGCGCCACCTAGTGCCGG | - | 6.08 | | INSM1 | MA0155.1 | chr17:80733111-80733123 | TGCCTGGGGGCG | + | 6.14 |
|
| | 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 |
| GH17I082774 | chr17 | 80732387 | 80734090 |
|
Enhancer Sequence | AATAGTGGAG GGAAGGTCGC AGATAAACAT GTGAACAAAG GTCTCTGGTT TTCCTAGGCA 60
GAGGACCCTG CGGCCTTCCG CAGTGTTTTT GTCCCTGGGT ACTTGAGATC AGGGAGTGGT 120
GATGACTCTT AAGGAGCATG CTGCCTTCAA GCATCTGTTT AACAAAGCAC ATCTTGCACC 180
GCCCTTAATC CATTTACCCC TGAGTGGACA CAGCACATGT TTCAGAGAGC ACGGAGTTGG 240
GGGTAAGGTT ATAGATTAAC AGCATCCCAA GGCAGAAGAA TTTTTCTTAG TACAGAACAA 300
AATCGAGTCT CCTATGTCTA CTTCTTTCTA CACAGACACA GTAACAAACT GATGTCTCTT 360
TCTTTTCCCC ACATTTCCCC CTTTTCTATT CGACAAAACC GCCATCGTCA TCATGGCCCG 420
TTCTCAATGA GCTGTTGGGT ACACCTCCCA GACGGGGTGG CAGCCGGGCA GAGGGGCTCC 480
TCACTTCCCA GACTTGGCGG CCGGGCAGAG GCACCCCCCA CCTCCCAGAC GGAGCGGCGG 540
CCGGGCGGGG GCTGCCCCCC ACCCGAGTGT GTCTACCTGT CGTTTGTGGT GGGACATTTA 600
GACTGCTGCC CTCCCAATTT GGTATTAAAA CTCAATATTG CAAACAGTCC ACGTAAAATT 660
GTGTACCGTT CTGACTGATT TCTAGGGATG AGTTTCTACA AGTGGAACGC ACGTTTTCAG 720
GGTCTGAATG CAATTACTGG AGAGGCTGAA CAAGTTGGAA GTTCTTTCCC CGTCTTTTCC 780
AGTTGGGTCA AACCTTAAGA ATGTTTGCCA ACTTCGTTCA ATGGGAAATA GTATCTGCTT 840
TTATTCTTAC TTTTCTTAGC AGCAGTACTG AGGGTTGCGT AGATTTTTGC CGAGCTTGGC 900
TCTGTGGAGT GCGGTGCCTG TGGGCCAGGA GGCACCATCT GAGTACTTCT CCCTCCGTGG 960
GGTCCTCCGG GAAAAGAGCG CGCTGGCTCG GGATCCCGGG CGGACTCCCG GCGAGACACC 1020
GCAGCGCCAC CTAGTGCCGG GATGAGCAGG TGCTTTTCGG CCGAGCCAGT TTCCGTGCAG 1080
AACACCTGAG CCTGGGATCC AGGAGAGGTG GTGCCTGGGG GCGTCGGTGC CGTGGAGCCT 1140
TTCTCCCCCT TGGTCTCGCA CACTCTCGCA CACTGATTCT CAAGAGTGTT TGAGAATGGC 1200
GGATGCCGTC AGTGGAAGAG CTCTTACAGG TGCTTGGCCG GTTCCCTCGA CACCTCCCAG 1260
ACTCACCGCA GGTTCTGAGT TTCCTGTACT TCTCAGACCC CTTTTTGGTG AGGATTGTTC 1320
AGGTAAGGCC AGGGCTGCGA GGGGTCCTGT GCCAGCATTT GTCTGCAGTA CAGGTTCGTT 1380
TTCTGCTCTC CAGGGAGGAG CAGCCTGCTC TAGCCCACTT TGCTCTCAGG ATTGAATGCT 1440
TCTCCCTGTA TCACTGGCGG CTCTACAGCT GCACCCGTCT CCCTTGATTA ACTGAGCTTG 1500
CCAACATCCA CAGCGCTGTA GGTGGTGCTT GGTGTTACAG TGTTGCTAGA ACATGCAGAT 1560
TGAGTGCTGC CTTAGAAACC CACAGGAAGG GGAACATCAC ACTCTGGGGA CTGTTGTGGG 1620
GTGGGGGGAG GGGGGAGGGA TAGCATTGGG 1650
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