Tag | Content |
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EnhancerAtlas ID | HS108-41590 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:130976420-130980500 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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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 | RARA(var.2) | MA0730.1 | chr9:130980478-130980495 | TGACCCTCCTTTGACCT | - | 6.74 | 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 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_65793 | chr9:130976260-130978472 | Pancreatic_islets | SE_65793 | chr9:130978750-130979599 | Pancreatic_islets | SE_65793 | chr9:130979969-130982022 | Pancreatic_islets |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I128214 | chr9 | 130976758 | 130979266 |
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Enhancer Sequence | GAAACCCACC GTCCAACTCT CTCCCCGCTG CCTCTTCTGG TGACGAGGCT GTGGGAGTCC 60 AGCCTGTGGT CTCAGCATGC CCAGCAAGCT ATCGTTATTT ATAATCATAG TAGCCACGAT 120 TGGTTCAGCC ATCAGTCTGT ATAAGCCTCA CAGCAACCCA TTTTACTGAT GTGGAAACTG 180 AGGCTCAGAG AGGTATGGTC ATTTGTGCAC AGCCACACAG CTCCTACATG ACAGCTCAGA 240 CATTCAATGT GGGGTCCATC TGACATCAGA GCCCAAAAAA GAGGAGGCAT AGAAGAATGA 300 CCGGCACTGG GTGCACGCCC AGTTAAGCAC GTTACTTCCT GGGGTCATTT GCATTCAGCA 360 GGGCCTGGGA ACCAGGATCC CAGAGCTCTG ATCCCAAGTC TCAGGTCCTA GAGTAGGGGT 420 AGGGGTAGGG GTCACATCAG CCCTTGGGTT CAGTTTCTCC AGACCCCTCT CACGGTGACA 480 ACTCCAGTTC AGACAGGGAG TGTGGCATTT GGGGTTCCTG AGAGGTGTTT GTTTCGTCCC 540 CTCATGTTTC ACGTTTGAAG GTGCCTCTGC AGATGGCCAG GCACAGCCTC CCTGGGAACC 600 CACCATCTGC TCCAAATGAG TGGGGAGAAC TGGCATGCCA GCAGCCGCCC CTCCCACGCT 660 GGGCACAGCA CGCGGCCTCC GAGGCTGGTG GGCCTGATAC TTTTCTCTGG GCACCTGTTC 720 TGTCCTCCCT TAGCCTAACC AGGAGCTGGA GGCTGGATCT AGTCTGGATC CCCACTGGGG 780 AGAAGGAGGG CCACCTAGGG GACCCTTAAA CAGAGGGCTA AAGTGGGACA GTGTGTCCAG 840 GTGAAAGGGA AGAGCTAGGG AGCTGCTGAG TCATGCACAT TCCTTCTCGT GTTGCCTGCA 900 CGCCTACTAC GTGCGGGGCC TGTGCCAGGC AGGAACCCGG AAGTGAGTGA GGAGCTCATT 960 GTCCGGACCT GGGGACCTGC TGGTCCTCCC CACTGTCAGT CCAGACGTGA GACTGGGAAG 1020 CAGACCTCTC GGGTCCTGGC ACCAGGCACC AGGCCAAGGA AAGGCCAATG TAGGATTCGA 1080 TGAAGGAGCC AGCCTGGCAC TGGCTCCTCA GCATGGGGCA GATGGTCCTT AAACTTAACA 1140 CGGAGTGTGG AAACCACCTG AGGATCCATT TAAAACCCAG ATTCTGCCTC CCCATGAAGC 1200 CCTCTTGAGA TTCTAGCCCA GCATGCCTGA GGAGCATGCG TCTGGACAAA CTACCCAAGG 1260 CATTCTGATG CAGGCCGCGT GAGGGCCTCA CTTTGAGAAC CTGGGCCATG ACAGAGATGG 1320 GCCACCTCCC CATCTGGGCA CCAGGAGATC TTGGCTCTGG GAGGGGTTGA CCCCCAGACA 1380 TGGCCCTGCC TCTAGTCTCT GCTTCCCAGA AGCTACTTGC CCTTTAAGTA GCCCTGGGGA 1440 GGCAGCAGGC AGCTGGCCCA GACCCTGACC ACCCAGCATT CTTGCCAGCT GGGCCCTGGG 1500 CTCCCCACAC CCGCTATGTG GCACCTTGGA GACCTCCACC CCTCAGGCTC ACCAGGGCTG 1560 CGTGGGCCTG TCTGCTCAAG GAGAGGCCTC TCAGGGAAGA ACTCCAGGGA AAGTCCACGT 1620 CTCTGTGTGG GGGACTCTTT GTGGGGAGTC CCATCCTTTC CAGCCCCTCC TGCAGTTTCC 1680 ATGGCAACTA CTGTTGCCAT GGTGTTGCTG GTGAGGAGCT GGTGGAGAAG AGGGTGGACC 1740 CCCGGCCCCC ACACCCACCC CAGCTTCTAT GAGAACAGCT GTTCTATCTC CACAGCCCTG 1800 GGGGACTCCC AAAACTGGAA GTCACGCCCC CAAAGGAGTC TTTGAGTAAA GGATGGGAGA 1860 GATTGAGACC GGAAGTCCTC CCACCCCCCA GCAAACCCCC TCCCTCTGTG CCGCCTGGCA 1920 CACCTCTGTT CTAGCACATA CCACGCTGCA TTGCATTATC TGTTTACTTG TCTGTCTCTC 1980 CCACCACACT GTGAGTTCCT CAGGGTGGGA ACTGTCTGAC TCATCATCTC CCATCCCCAG 2040 AGCCCGGCAC AGGGCCCGGC ACAGACTGAA TTTAATTGAA TTACATAAAA AGCCAAGTCT 2100 GGCTTCTTGG GTTTGAGACA GCACCATTGA ATGAGGAAGT TTCCAGGCTG AGGGTCCAAC 2160 AGACACTCAG CTTTGAATCC CCACTCTGCT GTGTGACCTT GGGTGAGTCA CTTCACCTCT 2220 CTGAGCCTCA GCTGCTTCCT CTGTAAAATG ATAATCTCTA TATCAGAGCA CAGATTCGAG 2280 GACTTGGAGA TTCAATCAGA ATTTATTGAG TGCCCCTTGT GTGCTAAGCC CTGTCCTGGG 2340 CACTGGGATA CAGTGGCAGA CAGAAAGAGG CTGCCCTGCT CACTGTCTGG CAAGAATGAA 2400 AAGCATTTGC CTGGTGCGCA GAAATGATGA ATATACACAG GGCTTACCAT CCTTCTCCTT 2460 CTCCAGTATA ATTCCTGACT CCTCCCCAGC AGCGTCCACT TCCCCAGACG TGAGGCAGTG 2520 GAGAGGCTTC AAGAGGGGGC TTTGAACCTA GGAGCTCTGG GTCTAGTCTG TTGTACCTAA 2580 GACCCTTAGC TCCTGACCCT GGGGTGCAAG AAGACTTGTG AGTCTGGGTC AGGCTCTGGG 2640 CTGGGAGCAA GAGACCTGGG TTCCACCTCT GGCTCTGTAG AGCTTGAATG TATCTTTTTC 2700 CCTCCCTGGG CCTCTCCATG AATAAGGCGC TGGCTGTGTC TCAATGGTCC CTCGGGCTTC 2760 AACCTGTTCC CCCCTTTCCT GGGCCCTGGA GATCCCATGA CTGGCAATTC TGACATCCTG 2820 ATTCCTGGAG AGGCCTTCAC CCTTGTGCTT GCGCCAGCTG GAGGGTGGTG CAGAGGGAGG 2880 TGGATGAAAA GAGCTGACTG GACAGAGAAC CGGCACCCAC AAGAGTCAGC CAAAAGGACA 2940 GCTGAGGTTG ACATTGGCAC GAGCAGATGT CTAAGCTATA GACTGTCAGG TCTGGGGACG 3000 GGGGATGACT TTGGGACCTC TCAGTCCAGT CCTTCAAAGG CGGCTCGGTT CACAGGGGGC 3060 TGAAGGGCAG GGGAGTGTCA CTGCAGAGTC AAATATATCC GAGACCAGGG TCTGCTCTGC 3120 CAGATACTGG CTGTGCAACC TGAATGTCTC TAAGGTGCAG CTCCCTCATC TGCAAAATGG 3180 GGGTAATAAC AGCACCTGCC TCATGGGGCT ACAGTATGGA GCCCCACTAA GCGCCTGGCA 3240 TGCAGTAGGC ACTAAGAAGC ATGAGTTTTT TTGTTTCTTT GTGGGTTTTT TTGAGGTGGA 3300 GTTTTGCTCT TGTCGCCTAG GCTGGAGTGC AATGGCGCGA TCTTGGCTCA CCGTAACCTC 3360 CGCCTCCCGG GTTCAAACAA TTCTCCTGCC TCAGCCTCCC AAATAGCTGA GATTACAGGT 3420 GCCTGACACC CCGCCGGCTA ATTTTTTTGT ATTTTTAGTA GAGACAGGGT TTCACCATGT 3480 TGGCCAGGCT GGTCTCAAAC TCCTGACCTC AGGTGATCCG CCCGCCTCAG CCTCCAAAGT 3540 GCTGGGATTA CAGGCGTGAG CCACCGCGCC CGGCCCATGA GTCCTTTTCC TTGCCACCTC 3600 CTTCCCCACT CTTCTTCAAC CCTAGCCATA TGGAGCCTGG AGAAGGGGAA GTGAGATGCT 3660 GCCCTGCCCC ACAGCGGAAG GGAGGGGAGA AGTTACAGCT CTGTTTCCTG GGATCCACTC 3720 TGTGGGCATT GGACACATAG GCATGTGGGA GACCCCATGC CTCAGTTTTC TGGGGCTGAA 3780 TGGCCGTGGC TGAGTTGGGG CAGGGACTTC CTATTGGTTC AAAACCAACA CAGGACGTAT 3840 CTAGGAGTTG ATCCAGTCTC TTGGCAGCTC AGATGCATAA ATTCTGTGAC CCAGGCGACT 3900 TGAGGAAAAG TATTTTCCAC CTTTCTGGGC TGCCATATGC TCTTAGTTAC CTGAAGCCCC 3960 TGGGCTAAGG AGCGGTGGAG CCAGCACTTT GGAAGGAGCT TTGGCTTTCC CAGGGGCCGG 4020 ACAGGTACCC CTGGGACAGA GGGCGCCCCC TCATATCTTG ACCCTCCTTT GACCTCCAAC 4080
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