Tag | Content |
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EnhancerAtlas ID | HS187-25297 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr9:126970620-126971860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:126971371-126971383 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr9:126971375-126971387 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr9:126971379-126971391 | GTTTGTTTGTTT | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr9:126970748-126970763 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr9:126971780-126971801 | CTTCCCCTCCCTTCCTCCTCC | - | 8.55 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09686 | chr9:126970556-126971701 | CD14 | SE_10789 | chr9:126970699-126972321 | CD19_Primary | SE_59974 | chr9:126945864-126986288 | Ly4 | SE_60868 | chr9:126958636-126982030 | DHL6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I124207 | chr9 | 126970242 | 126972282 |
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Enhancer Sequence | TCAAGTGATT CTCCTGCCTC AACCTCCCAA GTAATTGGGA TTACAGGTGC ACACCACCAC 60 GCCTGGCTAA TTTTTTTGTG TGTATTTTTA GTAGAGACGG GGTTTTGCCA TGTTGGCCAG 120 GCTGGTCTTG AACTCCTGAC CTCAAGTGAT CCACCTGCCT TGGCCCCCCA AAGTGCTGGG 180 ATTACAGGTG TGAGCCACCG CGCCCGGCCC AAAGACCCTT TTTCTAAATA AAGCTACATT 240 CACAGGTTCT GGGGGGTTTG GCTATGGACA TATATCTTTG AGAGCACCAT TCAATTTACT 300 ACACCCGGTG ACTTCCTGAC TCTATGTGCC TGTGCCACCC CACCCAAGTG AGTATCACTG 360 GAGAAAATCA CACAGCTAAG CTTCCGGGTT TCACTCTAAA TTCATGACCA CAGACCTCAA 420 ATGGGCACCT CAAGCTGCCC CACAGAGCCT CCTGTGTTTC TCTTTTCTGG AGTAAGCATT 480 TCCTATCTTT TCACTTTTCA AATGTATCAC CCCCTTGCCA CCCCATCTCT CTCAATAGGT 540 AACCATGCCC CAAACACCAC TGATGGAACA GATGCTCAAG AGGCGTGACT GCCTTCTTGG 600 TCTTGCCCCA TCCCTGTGAA CCTATCTCAT CTGCCTTGGT CTTTGTGTCC TCCTTCCTGG 660 CATCCAGAGG CCATGTCCCT TCTCTTCCCA GAGGCCAATG CCATGACTTG TGCTCTGAAT 720 CCCATTCCTT CTCGCCTTTT GTTTTTTGGT TGTTTGTTTG TTTGTTTGTT TGAGACACAG 780 TCACTCTGTA GCCCATGCCT GTGTCATGCA GTGGTGCGAT CTCGGCTTGC TGCAACCTCT 840 GCCTCCTGGG TTCAAGCGAT TCTCCTACCT CAGCCTCCCA AGTAACTGGG ACTATGAGCG 900 CATGCCACCA CGTCCGGACA ATTTTTGTAT TTTTGGTAGA GACTGTCTCT ACCAGTCTTG 960 AACTCCTGAC CACCTGATCC GCCCACCTCA GCTTCCTGAA GTGCTGGGAT TACAGGAGTG 1020 AGCCGCTGCA TCCACCCCGC TTCTTGCCTT TTTAAGGGCT TGAATCCTAT TGTGTGTTCC 1080 TGATCAGTAC CTCCCTCTCC TGTTAGCCCA CAGACCTGCT CCGGGGTGTT GCATCTTGAA 1140 AACTCCTCCC ACCTTGGGCC CTTCCCCTCC CTTCCTCCTC CCATTATCTT TGTAGAGCTG 1200 CCTCTGACTC CTCACCTCCC ATCTTCCTTT CGTTAGCCCA 1240
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