Tag | Content |
---|
EnhancerAtlas ID | HS095-16716 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:109588170-109589520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox6 | MA0515.1 | chr2:109589188-109589198 | AAAACAATGG | - | 6.02 | Stat6 | MA0520.1 | chr2:109588727-109588742 | CTGTTCCACAGAACT | + | 6.08 | Stat6 | MA0520.1 | chr2:109589393-109589408 | ATTTCTTAGGAAGAG | - | 6.35 | TCF3 | MA0522.2 | chr2:109589413-109589423 | AGCAGGTGTT | - | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26844 | chr2:109586492-109590435 | Esophagus |
|
| 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 |
GH02I108971 | chr2 | 109587479 | 109589380 |
|
Enhancer Sequence | TTGGCATTAG AAGTCAGGTG TTGTGGTTTA TAACACATAC ACAAACTCTT TGATACCACC 60 TTCAAAAGGT GGAGCCTAAT TCCTCTCCCT GTGTGAACGG GCTGGATTTT AGTGACTCGT 120 TTCTAGCCAA CAGAAAAAAG GGCAGAAGAG ACGGTGCAAT TACAGAGACC AGGTCACCAA 180 AGGCACTGAG CTTCCTGCTG TGCCGTGGCT GCTGCTCAGT CACATAGGGG CAACAGAGGA 240 GCAGCCGTGG GGAGCTCCCG TGGCCCGGAG CTGAGGCCTC CTGCCGCAGC CACTTGCGAG 300 GCCTCTGGAT GTGGGTCCTC CAGCCTGGCC TGGCCCGCAG ATGTTGCAGC CCAGCCGACT 360 GCAGCCTCAG GAAGGACACT GAGCCAGAAC CACCCAGCGG AGCCGCTCCC TGATTCCTGA 420 CCCTCAAAAT CTGTGGGATG GTCACATTTG TTGTTTTAAG CAGTTACATT TGGGAGTCAT 480 TTATTACACA GCACAGATGA CTAATACGCC TTCCAGTCCT TTGCTGTTTC AGCCACACCC 540 CTGTAAGAGA CCAACTTCTG TTCCACAGAA CTTCAATAGC CATGCCGGCC CAGTTCTCGA 600 CAAGCTTAGG ATTGAACACA GACAATGATG ACCAAATCAA AACAGGGGCA GGGCACTGCA 660 TGGTGTGGTC TCCACTCCTT CCTCACGGGC CCTGGAGCCC TTGCCCAACC CTCCTGGCTG 720 GCTTTCATGC CAACGTGCCA GACACTGCCC TTTCCAATCC TGCCCGCTGT GGGAGTGCCG 780 GGGCAGGGCA AGGTCAGGCT GCAACGGGCC GAGGCAGCCT AGGAAAAAAG AGATTGTAGG 840 TGACCTGGGT TCAGAAGCTG GTGCCTTGCC CTGCACGCCA AGTGTTGGTA AAACAAGTGT 900 CTGCACAAGG GTGACGGGTG TCTTCCCCAC TCTGCTTGCC TTGTAGCTAT GGCTGTGATC 960 AGAGAACTTG ACGTGATCAT TTGAAAAATA AGCAGCCCTC ATCTGATTTG TCAGTCACAA 1020 AACAATGGCT CACAGCCCAT GCAGATGCTG AGACTCAGAA GGGGGTGAGG ACCGGGGGGC 1080 CTCCGGCAGG GGCGTTCACT CTTCCTCCAA CCTCCCCAAC CTTGGCTAGC TGGATTCTCC 1140 TCTTTGCCTT CTTGAACTTT CTTCTAGAGC TCTCTGAGCT GGGCACGCCC AGAACAAGGC 1200 AACCTGTGCT CCAAGTCCAA AGAATTTCTT AGGAAGAGGT CTCAGCAGGT GTTTATTTTT 1260 TTATTTATTT TAATTGAATT TTTTTTTTTG AGATGGAGTT TCACTCTTGT CATCCAGGCT 1320 AGACTGCAGT GGCGCAATTT CAGCTCACCG 1350
|