Tag | Content |
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EnhancerAtlas ID | HS187-07572 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr14:69821190-69822430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX2 | MA0600.2 | chr14:69821750-69821766 | TGTTCCCATGGAAACC | + | 6.01 | RFX2 | MA0600.2 | chr14:69821750-69821766 | TGTTCCCATGGAAACC | - | 6.12 | RFX5 | MA0510.2 | chr14:69821750-69821766 | TGTTCCCATGGAAACC | + | 6.11 | ZNF263 | MA0528.1 | chr14:69822245-69822266 | TCCTCTTGCTTGCTCTCCTCC | - | 6.16 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59418 | chr14:69802940-69828523 | Ly3 |
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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 |
GH14I069353 | chr14 | 69820701 | 69823060 |
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Enhancer Sequence | ACCAGCGCCT TCCTTTCTGC CTCCAGGCCT AGCCCTTCAG CACACCCTCC CCCGCCTCGT 60 GGGGAAAGTC CGGGCCTCCT TTCTGTAAAA GTGAAACTGA ACATGCTCAA GTCTAGCCCT 120 GTCCTGCACC TGGTAGCTTG CTCGTCGGCC TCCATGCCCT GTGGTGCCCC AGGAACTCCT 180 GACTGCTCTG GTGGGGGCCA ACAGGTGGCC CTACTGCAAG GGCAGGCCTT GGACCAAAAC 240 CAGGAATCAG CACAGGTCAG GTGGAGCCCA GGCTCCTGTG GCCTCATTAT GGGATTCTAC 300 TTGGGGCTTA GAAATGGAAA GCAAATTGCT TCTCCAAATA GGTATTGCCC TGCCGCCGTG 360 CTTGCCTTTA GCCAGCCCTC TCTCCTTCCC TGTGAGCCAG GCCTGTCCCC TCGGAGCTGC 420 CCTCCCCTGC TCTACCACAC AAGAAGGCAG TGGTACAAAT TCAGGCAGGA CATACTTCCT 480 GGGTAAAAAC AGCAAAATAA TTCTGAAAAG AGTCTTACCA GACCAGCTTT GCTTGATTGG 540 GTAGCAGATG CTCTGCCTAA TGTTCCCATG GAAACCAATG GAAAACCCCC ACCATGTCTG 600 TGATCAGAAG CTGAACCTAC CCAGGTAAAA ATAAACGCTG CTTCAACATA CATATGAACT 660 GCAGCTGGCA GGCCAGCACA CCACTAGCCT CTCCTGGACG CAACCATTTC TGCCCTCAGC 720 CCCACTTTGC CGTGGGGCTG CTGATCTGGA GTTACCCAGA ACTTCTGACC CCTGGGCCTG 780 AGGAGCCTGG AGCAAAGCCC TAGCTGGCTG CAGAGAATAC ACCTTGGCTA CAATGTCCAG 840 CTTGGTCTGG GCTTAGGAGC AAGTCACTGT AAAAGACCTT GGCTGCAGCC TCCATTCCCC 900 CATCCACCCC TCCGTCCTCT CAGGGAGCAC AGCCCACCAC CCACCGCCTA CTCAGGGCTC 960 CCTCCTGGCG CGCTGAGCCC CATTTCCACT CTCCATCTAT TTTCACCCTC AGCCTTGGAG 1020 GGCTCTGGTG CTTGCTTCTC CTGAGTCAGG CTCTCTCCTC TTGCTTGCTC TCCTCCAAAC 1080 CTACCTCTCC CAAAGCCCAT TTTCTGTGCC ACCCAGTTTT TTCCCTAGGA GATAAGGCTG 1140 TCAGCCTTTA GCCAGGCCCT GGAGGAATCA GCAAAAGCCC CAGGCTGGGT ATTAACAGTT 1200 ACGTCACTGG CAGGAGAGTC CCCCGAAAGC CTATGGGCAG 1240
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