Tag | Content |
---|
EnhancerAtlas ID | HS062-06722 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr17:4315330-4317150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:4316664-4316683 | CAGCGCCACCTGGTGGCCA | - | 9.86 | EWSR1-FLI1 | MA0149.1 | chr17:4316835-4316853 | TCTTCCTTCCTTCCTTCC | - | 10.05 | EWSR1-FLI1 | MA0149.1 | chr17:4316886-4316904 | CCTCCCTCCCTCCCTTCC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr17:4316831-4316849 | TCCTTCTTCCTTCCTTCC | - | 7.2 | EWSR1-FLI1 | MA0149.1 | chr17:4316839-4316857 | CCTTCCTTCCTTCCTTTC | - | 9.6 | IRF1 | MA0050.2 | chr17:4316090-4316111 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | IRF1 | MA0050.2 | chr17:4316817-4316838 | GCTTGCTTTCTCTTTCCTTCT | + | 6.71 | ZNF263 | MA0528.1 | chr17:4316823-4316844 | TTTCTCTTTCCTTCTTCCTTC | - | 6.13 | ZNF263 | MA0528.1 | chr17:4316835-4316856 | TCTTCCTTCCTTCCTTCCTTT | - | 6.24 | ZNF263 | MA0528.1 | chr17:4316881-4316902 | TTTTCCCTCCCTCCCTCCCTT | - | 6.39 | ZNF263 | MA0528.1 | chr17:4316891-4316912 | CTCCCTCCCTTCCTCTCCTTC | - | 6.39 | ZNF263 | MA0528.1 | chr17:4316877-4316898 | CTCTTTTTCCCTCCCTCCCTC | - | 6.49 | ZNF263 | MA0528.1 | chr17:4316894-4316915 | CCTCCCTTCCTCTCCTTCTCT | - | 6.49 | ZNF263 | MA0528.1 | chr17:4316885-4316906 | CCCTCCCTCCCTCCCTTCCTC | - | 6.54 | ZNF263 | MA0528.1 | chr17:4316831-4316852 | TCCTTCTTCCTTCCTTCCTTC | - | 6.63 | ZNF263 | MA0528.1 | chr17:4316928-4316949 | TCCCTCCCCCCTCCCTCCCTT | - | 6.69 | ZNF263 | MA0528.1 | chr17:4316361-4316382 | TCTTCCCCTTTTCCGTCCTCC | - | 6.89 | ZNF263 | MA0528.1 | chr17:4316932-4316953 | TCCCCCCTCCCTCCCTTCTCT | - | 6.8 | ZNF263 | MA0528.1 | chr17:4316886-4316907 | CCTCCCTCCCTCCCTTCCTCT | - | 6.99 | ZNF263 | MA0528.1 | chr17:4316924-4316945 | TCCCTCCCTCCCCCCTCCCTC | - | 7.3 | ZNF263 | MA0528.1 | chr17:4316364-4316385 | TCCCCTTTTCCGTCCTCCTTC | - | 7.49 | Zfx | MA0146.2 | chr17:4315837-4315851 | GAGGCCGAGGCGGG | - | 6.01 |
|
| 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 |
GH17I004412 | chr17 | 4316139 | 4317190 |
|
Enhancer Sequence | GGTCTTGAAC TCCAGACCTC AAGTGATCCA CCCACCTCGG CCTCCCAAAG TGCTGGGATT 60 ACAGGCGTGA GCCACTGCGC CCGGCCAACT TTACCCATTT CCACCTTTGA TGTGTGCAGT 120 AAAATGCATT CTTGCTGGTG ATTTGCGGTC TTGGGCTTCT GGGCCAAGCG GAGCTCTGCC 180 TTGGACGCAT GCGCAGCAGA TGATGGCCCG TGTTTTTTGT ACGTGTGTGT TTTGCATTAA 240 GGAAGGAAAG TGATGACCTT CACGGGTCAG CATCTTTCCC TGAGTCTCCT CTCTTAAATG 300 AATACTTGAG ATCCCAAGTG GCTTATCATG AGTTTTCCTC TATATCAAGG GTCTGTGAAC 360 TCTGGCCTGC TGGAAGCATG GCTGATGGCC TGTTTTTTTT GTTTTTTTTT GGCCCCTGAA 420 CTAATAACGG TTTTCACATT TGTTTGTTTA AAAAAATACA TTTCTGGCTG GGCGCGGTGC 480 CTCACGCCTG TAATCCTAGC ACTTTGGGAG GCCGAGGCGG GTGGATCACC TGAGGTCGGT 540 AGTTTGAGAC CAGCCTGACC AACATGGAGA AACCCCATCT CTACTAAAAA TACAAAATTA 600 ACAGGGTGTA GTGGCAGGCA CCTGTAATCC CAGCTACTTG GGAGGCTGAG GCAGGAGAAT 660 CACTTGAACC CGGGAGGAGG AGGTTGCGGT GAGCCAAGAT CGCGCCATTG CAATCCAGCC 720 TGGGCAACAA CAGCGAAACA TCGTCTCAAA AAAAAAAAAA AAAAAAAAAA AGAAAGAAAG 780 AAAAGAAAAA AAGAAAAAAA AAAGATTGAT TTCCCCACCT CCCCACCTCT TCCACGAGTT 840 CCCCAAGCCC TGCAAGATGA CTTCGATGGG ATACAATTGT TTCCACCTCA TCACAGCAGA 900 ATGATAATGC CTATAGCCTG TCAATGGCAA GTTCTCGAAT GTGTGGGCAC CAGGAACACA 960 CCCCGGAAGC CACATGTCCT TGCCCCAAGG GAAGGGCCCT GGAGAGCAGA AGAGAGGAGG 1020 AAAGTTGAGC CTCTTCCCCT TTTCCGTCCT CCTTCCTCCT GCCCTGATTC TGCCCACAGA 1080 GGAAGGGTCT GAGCTAGAGG AACCTGGACA GTGAATCCAC ACCCTATGGA CAGATGAGAA 1140 GACCGAGGCC AGAGACAACG CAGGGTCCGG CCCCTGGTCC TATGCCTGAT GCCTCTCACT 1200 GGAGACCCCT CCCCCACTTC AAGGTCGCCC CTAGAAGGCA AACGCTGAAG CCAAGTGTTC 1260 TTGGAGCGTC TCTTGGTGGA CGCTTCGGCC CTGCCACGGA ACGGCCCCTT AGTGAAGGTT 1320 CTCAGCTTAG ACTTCAGCGC CACCTGGTGG CCACCGGGCA TCAGACCTGG GACTTGCCTC 1380 GAGGGCTGCC AGAAACTTGA GTTTGTCCAC TCACATCACT GCATCCCGTG GAGAAGTCCC 1440 AGTGCCGACC TGCTTGCTTG CTTGCTTGCT TGCTTGCTTG CTTGCTTGCT TGCTTTCTCT 1500 TTCCTTCTTC CTTCCTTCCT TCCTTTCCTT TCTTTTCTTT TTTCTTTCTC TTTTTCCCTC 1560 CCTCCCTCCC TTCCTCTCCT TCTCTCTCTC TGTCTCCCTC CCTCCCCCCT CCCTCCCTTC 1620 TCTCTCTCTC TGTTTTTCTC TCTCTCTGTC TCTCCTGCCT TCCCGCTTTC TTTCTTTCTT 1680 TCTTTTTTTT TGTTTTTGAG ACGGAGTCTC GCTGACTCCC ATGCTGGAGT GCAGTGGCGC 1740 GATCTCCGCT CACTGCAAGC TCTGCCTCCC GAGTAGCTGG GACTACAGGC GCCCGCCTCC 1800 ACGCCCGGCT AATTTTTTGT 1820
|