Tag | Content |
---|
EnhancerAtlas ID | HS092-38891 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:130976440-130979730 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr9:130977353-130977365 | AACCCGGAAGTG | + | 6.74 | ELF1 | MA0473.2 | chr9:130977353-130977365 | AACCCGGAAGTG | + | 7.22 | ELF3 | MA0640.1 | chr9:130977353-130977366 | AACCCGGAAGTGA | + | 7.22 | ELF4 | MA0641.1 | chr9:130977353-130977365 | AACCCGGAAGTG | + | 7.22 | ELF5 | MA0136.2 | chr9:130977354-130977365 | ACCCGGAAGTG | + | 6.32 | FOXP1 | MA0481.2 | chr9:130978377-130978389 | ATCTGTTTACTT | - | 6.74 | FOXP2 | MA0593.1 | chr9:130978378-130978389 | TCTGTTTACTT | - | 6.32 | GLIS3 | MA0737.1 | chr9:130978056-130978070 | CTTTGTGGGGAGTC | - | 6.16 | MSC | MA0665.1 | chr9:130978193-130978203 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr9:130978193-130978203 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr9:130978193-130978203 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr9:130978193-130978203 | AACAGCTGTT | - | 6.02 | NFE2L1 | MA0089.2 | chr9:130977281-130977296 | GCTGCTGAGTCATGC | - | 6.64 | Nfe2l2 | MA0150.2 | chr9:130977283-130977298 | TGCTGAGTCATGCAC | - | 6.66 | PHOX2A | MA0713.1 | chr9:130978492-130978503 | TAATTGAATTA | - | 6.14 | Phox2b | MA0681.1 | chr9:130978492-130978503 | TAATTGAATTA | - | 6.14 | RFX1 | MA0509.2 | chr9:130978093-130978109 | AGTTTCCATGGCAACT | - | 6.33 | RFX1 | MA0509.2 | chr9:130978093-130978109 | AGTTTCCATGGCAACT | + | 6.35 | RFX2 | MA0600.2 | chr9:130978093-130978109 | AGTTTCCATGGCAACT | + | 6.67 | RFX2 | MA0600.2 | chr9:130978093-130978109 | AGTTTCCATGGCAACT | - | 6.72 | RFX5 | MA0510.2 | chr9:130978093-130978109 | AGTTTCCATGGCAACT | - | 6.61 | RFX5 | MA0510.2 | chr9:130978093-130978109 | AGTTTCCATGGCAACT | + | 6.6 | STAT3 | MA0144.2 | chr9:130977821-130977832 | CTTCCCAGAAG | - | 6.14 | ZBTB7A | MA0750.2 | chr9:130977354-130977367 | ACCCGGAAGTGAG | + | 6.15 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_65793 | chr9:130976260-130978472 | Pancreatic_islets | SE_65793 | chr9:130978750-130979599 | Pancreatic_islets |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr9 | 130976556 | 130978716 | chr9 | 130979056 | 130979435 | chr9 | 130976600 | 130977800 | chr9 | 130978792 | 130978931 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I128214 | chr9 | 130976758 | 130979266 |
|
Enhancer Sequence | CTCCCCGCTG CCTCTTCTGG TGACGAGGCT GTGGGAGTCC AGCCTGTGGT CTCAGCATGC 60 CCAGCAAGCT ATCGTTATTT ATAATCATAG TAGCCACGAT TGGTTCAGCC ATCAGTCTGT 120 ATAAGCCTCA CAGCAACCCA TTTTACTGAT GTGGAAACTG AGGCTCAGAG AGGTATGGTC 180 ATTTGTGCAC AGCCACACAG CTCCTACATG ACAGCTCAGA CATTCAATGT GGGGTCCATC 240 TGACATCAGA GCCCAAAAAA GAGGAGGCAT AGAAGAATGA CCGGCACTGG GTGCACGCCC 300 AGTTAAGCAC GTTACTTCCT GGGGTCATTT GCATTCAGCA GGGCCTGGGA ACCAGGATCC 360 CAGAGCTCTG ATCCCAAGTC TCAGGTCCTA GAGTAGGGGT AGGGGTAGGG GTCACATCAG 420 CCCTTGGGTT CAGTTTCTCC AGACCCCTCT CACGGTGACA ACTCCAGTTC AGACAGGGAG 480 TGTGGCATTT GGGGTTCCTG AGAGGTGTTT GTTTCGTCCC CTCATGTTTC ACGTTTGAAG 540 GTGCCTCTGC AGATGGCCAG GCACAGCCTC CCTGGGAACC CACCATCTGC TCCAAATGAG 600 TGGGGAGAAC TGGCATGCCA GCAGCCGCCC CTCCCACGCT GGGCACAGCA CGCGGCCTCC 660 GAGGCTGGTG GGCCTGATAC TTTTCTCTGG GCACCTGTTC TGTCCTCCCT TAGCCTAACC 720 AGGAGCTGGA GGCTGGATCT AGTCTGGATC CCCACTGGGG AGAAGGAGGG CCACCTAGGG 780 GACCCTTAAA CAGAGGGCTA AAGTGGGACA GTGTGTCCAG GTGAAAGGGA AGAGCTAGGG 840 AGCTGCTGAG TCATGCACAT TCCTTCTCGT GTTGCCTGCA CGCCTACTAC GTGCGGGGCC 900 TGTGCCAGGC AGGAACCCGG AAGTGAGTGA GGAGCTCATT GTCCGGACCT GGGGACCTGC 960 TGGTCCTCCC CACTGTCAGT CCAGACGTGA GACTGGGAAG CAGACCTCTC GGGTCCTGGC 1020 ACCAGGCACC AGGCCAAGGA AAGGCCAATG TAGGATTCGA TGAAGGAGCC AGCCTGGCAC 1080 TGGCTCCTCA GCATGGGGCA GATGGTCCTT AAACTTAACA CGGAGTGTGG AAACCACCTG 1140 AGGATCCATT TAAAACCCAG ATTCTGCCTC CCCATGAAGC CCTCTTGAGA TTCTAGCCCA 1200 GCATGCCTGA GGAGCATGCG TCTGGACAAA CTACCCAAGG CATTCTGATG CAGGCCGCGT 1260 GAGGGCCTCA CTTTGAGAAC CTGGGCCATG ACAGAGATGG GCCACCTCCC CATCTGGGCA 1320 CCAGGAGATC TTGGCTCTGG GAGGGGTTGA CCCCCAGACA TGGCCCTGCC TCTAGTCTCT 1380 GCTTCCCAGA AGCTACTTGC CCTTTAAGTA GCCCTGGGGA GGCAGCAGGC AGCTGGCCCA 1440 GACCCTGACC ACCCAGCATT CTTGCCAGCT GGGCCCTGGG CTCCCCACAC CCGCTATGTG 1500 GCACCTTGGA GACCTCCACC CCTCAGGCTC ACCAGGGCTG CGTGGGCCTG TCTGCTCAAG 1560 GAGAGGCCTC TCAGGGAAGA ACTCCAGGGA AAGTCCACGT CTCTGTGTGG GGGACTCTTT 1620 GTGGGGAGTC CCATCCTTTC CAGCCCCTCC TGCAGTTTCC ATGGCAACTA CTGTTGCCAT 1680 GGTGTTGCTG GTGAGGAGCT GGTGGAGAAG AGGGTGGACC CCCGGCCCCC ACACCCACCC 1740 CAGCTTCTAT GAGAACAGCT GTTCTATCTC CACAGCCCTG GGGGACTCCC AAAACTGGAA 1800 GTCACGCCCC CAAAGGAGTC TTTGAGTAAA GGATGGGAGA GATTGAGACC GGAAGTCCTC 1860 CCACCCCCCA GCAAACCCCC TCCCTCTGTG CCGCCTGGCA CACCTCTGTT CTAGCACATA 1920 CCACGCTGCA TTGCATTATC TGTTTACTTG TCTGTCTCTC CCACCACACT GTGAGTTCCT 1980 CAGGGTGGGA ACTGTCTGAC TCATCATCTC CCATCCCCAG AGCCCGGCAC AGGGCCCGGC 2040 ACAGACTGAA TTTAATTGAA TTACATAAAA AGCCAAGTCT GGCTTCTTGG GTTTGAGACA 2100 GCACCATTGA ATGAGGAAGT TTCCAGGCTG AGGGTCCAAC AGACACTCAG CTTTGAATCC 2160 CCACTCTGCT GTGTGACCTT GGGTGAGTCA CTTCACCTCT CTGAGCCTCA GCTGCTTCCT 2220 CTGTAAAATG ATAATCTCTA TATCAGAGCA CAGATTCGAG GACTTGGAGA TTCAATCAGA 2280 ATTTATTGAG TGCCCCTTGT GTGCTAAGCC CTGTCCTGGG CACTGGGATA CAGTGGCAGA 2340 CAGAAAGAGG CTGCCCTGCT CACTGTCTGG CAAGAATGAA AAGCATTTGC CTGGTGCGCA 2400 GAAATGATGA ATATACACAG GGCTTACCAT CCTTCTCCTT CTCCAGTATA ATTCCTGACT 2460 CCTCCCCAGC AGCGTCCACT TCCCCAGACG TGAGGCAGTG GAGAGGCTTC AAGAGGGGGC 2520 TTTGAACCTA GGAGCTCTGG GTCTAGTCTG TTGTACCTAA GACCCTTAGC TCCTGACCCT 2580 GGGGTGCAAG AAGACTTGTG AGTCTGGGTC AGGCTCTGGG CTGGGAGCAA GAGACCTGGG 2640 TTCCACCTCT GGCTCTGTAG AGCTTGAATG TATCTTTTTC CCTCCCTGGG CCTCTCCATG 2700 AATAAGGCGC TGGCTGTGTC TCAATGGTCC CTCGGGCTTC AACCTGTTCC CCCCTTTCCT 2760 GGGCCCTGGA GATCCCATGA CTGGCAATTC TGACATCCTG ATTCCTGGAG AGGCCTTCAC 2820 CCTTGTGCTT GCGCCAGCTG GAGGGTGGTG CAGAGGGAGG TGGATGAAAA GAGCTGACTG 2880 GACAGAGAAC CGGCACCCAC AAGAGTCAGC CAAAAGGACA GCTGAGGTTG ACATTGGCAC 2940 GAGCAGATGT CTAAGCTATA GACTGTCAGG TCTGGGGACG GGGGATGACT TTGGGACCTC 3000 TCAGTCCAGT CCTTCAAAGG CGGCTCGGTT CACAGGGGGC TGAAGGGCAG GGGAGTGTCA 3060 CTGCAGAGTC AAATATATCC GAGACCAGGG TCTGCTCTGC CAGATACTGG CTGTGCAACC 3120 TGAATGTCTC TAAGGTGCAG CTCCCTCATC TGCAAAATGG GGGTAATAAC AGCACCTGCC 3180 TCATGGGGCT ACAGTATGGA GCCCCACTAA GCGCCTGGCA TGCAGTAGGC ACTAAGAAGC 3240 ATGAGTTTTT TTGTTTCTTT GTGGGTTTTT TTGAGGTGGA GTTTTGCTCT 3290
|