| Tag | Content |
|---|
EnhancerAtlas ID | HS091-49355 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chrX:41111680-41113370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:41113118-41113137 | TGCTGCCCTCTAGAGGCCG | - | 6.91 | | Foxd3 | MA0041.1 | chrX:41111705-41111717 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chrX:41111709-41111721 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chrX:41111713-41111725 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chrX:41113318-41113330 | GTTTGTTTGTTT | + | 6.32 | | ZNF263 | MA0528.1 | chrX:41112147-41112168 | TCCTTCCTTTCTGCCTCCTCA | - | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 41112099 | 41112200 | | chrX | 41112416 | 41113113 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI041253 | chrX | 41112254 | 41113453 |
|
Enhancer Sequence | GAGCCCAGCC TCAATAAATG TTTTTGTTTG TTTGTTTGTT TGTTTTTTGA GATGGAGTCT 60
CGCTCTGTTG CCCAGGCTGG AGTGCAGTGG TGCGATCTTG GCTCACTGCA ACCTCCACCT 120
CCCAGGTTCA AGTGATTCTC CTGCCTCAGC CTCTCAAGTA GCTGGGATTA AAGGCGCTGC 180
CACCATGTCC GGCTAATCTT TGTATTTTTA GTAGAGATGG GATTTCACCA TGTTGGCCAG 240
GCTGGTCTCG AACTTCTGAC CTCAAGTGAT CCACCTGCCT TGGCCTCCCA AAGTGCTGGG 300
ATTACAGGCA TGAGCCACCA CGCCCAGCCG CCTCAAATTT TTAAAAAAAC ATGTGCCTTC 360
CCCTGCACGT TGCTCCAGGG ACGTGCACAC ACACCCTCTG CCTGGCACAC CACAGCTGAC 420
AAGGGCTGAC AATAGTCAAT TTCATCAGAG TGCTTTTCTC ACCTAGATCC TTCCTTTCTG 480
CCTCCTCACC ACACCCCTTT ACCCACAAAC AGTGGGAGGG GAGCCCTGGA CACTCTCAGC 540
TTCCTCCTGC CCCTGAGTTC CAGCGATCAA AGATAAAATT GAAAACATTA GCTATGCCCA 600
CTGCTCCCTG GTGGAAGGCA GCCACCTTCT GAGGAGGTCC CATGGGAGAG TGAGTCCCCT 660
CCCCGTGCAT AACCCGACCC CCAAATTGGG GGCTCTTCAG ACCTCATCAG ATCCTGCACA 720
GGCCCCCCAG GATAGGTGCT TGGGGTGCAG CAGCTGGCCA AGGCGCTGTG CCTTGTTGTC 780
TAGGTGGTGT GCCCACCCGG GCTCCCGGTC CCGCCTGGTC ACAAGCATCC CCGCGTCAGC 840
TGATGAACAC CCCTGTCCAG CAGGTGCCAG ACACCCGAAA TCAAGAGGAG TGTCCTGTGC 900
TCCAGGAGCC TGAGAGGTGG CAAAGTCCCC GGGGGGAGGC GTGATGGTAG GGAAGGCTTC 960
TGACATACCT CTGCAGGGGC CAGGGCCCTG AGTCCCGGGT CCCCATGGTG TGTTTCTGTG 1020
TGAAGTCAGT GGCACTGCCA GCGCCGTGGT CATATTACCT AGGCCACAGC TGCCAGGCCT 1080
GCAAGCTCTT TCCTACTTCC CTTAGGTGCC CAGACCCAAA GTCAAGAGGA CCTTGACCCG 1140
TGGGGGTCGT GGGGAATGAA AACCGTCCTG CGAACTTGAA CTTCACTAGG GAGGCGGCGC 1200
TCTCTCTGCC CCGGTTCTAT CACGCGCATC CGTTAGGAAC TAAGCGGCAC CTGCGCGAGG 1260
CTAGGCTTGT TGACATATTT CTTGCTGGCG GCGTCCTCTC GCGTGGAGCA CGACTGCGCA 1320
AAGCGCCGAC AGTCCCCCGA GCGAGGACGG CAGCGAGACT CCGAAGCCCC CTTAGCAACC 1380
AAGCCGGTGC CGCTGCCCTT GCGCCGGGAC TGCAGCCGGG TCTTCCGAAG TGAGGATATG 1440
CTGCCCTCTA GAGGCCGCGG GGTGACATGG CCCATGAGGC TGTCTGGGCA GGGTGGGTTC 1500
GGGTGGGAGG AACCAAGGTG GACAAGCCTC GAAGTAAGAG ATCTGTTCAA GGTCACAGGG 1560
AGTCGGGACT CATGCGGAGG CACAGATCCA AGCTCTCTGT ACTGGGCCCT TTGGTATTCT 1620
GTTGGCTCCT ATTTTTTTGT TTGTTTGTTT TTTGTTTTTT GTTTTAGATG GAATCTCTGT 1680
AGCCCAGGCT 1690
|
